UCSC Genome Browser on Human (GRCh38/hg38)
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chr11:35,139,181-35,230,027 90,847 bp.
  
-   Custom Tracks
CSCC_F0209_N_E
CSCC_T0045_N
GAC_W0451_T_E
HCC_G0218_T_L
LUAD_X0687_T_L
LUSC_X0703_N_L
PTC_J0924_T
SCLC_X0608_T_E
CSCC_F0209_T_E
CSCC_T0045_T
GAC_W0505_N_E
HCC_G0224_N_L
LUAD_X0742_N_L
LUSC_X0703_T_L
PTC_J0925_N
SRCC_W0064_N_L
CSCC_F0287_N_E
ESCC_X0525_N_E
GAC_W0505_T_E
HCC_G0224_T_L
LUAD_X0742_T_L
LUSC_X0753_N_E
PTC_J0925_T
SRCC_W0064_T_L
CSCC_F0287_T_E
ESCC_X0525_T_E
GAC_W0620_N_L
HCC_G0228_N_E
LUAD_X0803_N_E
LUSC_X0753_T_E
SCLC_X0212_N_L
SRCC_W0158_N_L
CSCC_F0297_N_E
ESCC_X0601_N_E
GAC_W0620_T_L
HCC_G0228_T_E
LUAD_X0803_T_E
LUSC_X622_N_E
SCLC_X0212_T_L
SRCC_W0158_T_L
CSCC_F0297_T_E
ESCC_X0601_T_E
GAC_W0627_N_L
HCC_G0267_N_E
LUSC_8_N_L
LUSC_X622_T_E
SCLC_X0242_N_E
SRCC_W0207_N_L
CSCC_T0010_N
ESCC_X0702_N_L
GAC_W0627_T_L
HCC_G0267_T_E
LUSC_8_T_L
PTC_J0921_N
SCLC_X0242_T_E
SRCC_W0207_T_L
CSCC_T0010_T
ESCC_X0702_T_L
GAC_W0628_N_L
LUAD_X0147_N_L
LUSC_X0627_N_L
PTC_J0921_T
SCLC_X0272_N_L
CSCC_T0024_N
ESCC_X0724_N_E
GAC_W0628_T_L
LUAD_X0147_T_L
LUSC_X0627_T_L
PTC_J0924_N
SCLC_X0272_T_L
CSCC_T0024_T
ESCC_X0724_T_E
HCC_G0164_N_E
LUAD_X0668_N_E
SCLC_X0608_N_E
GAC_W0447_N_E
HCC_G0164_T_E
LUAD_X0668_T_E
GAC_W0447_T_E
HCC_G0213_N_L
LUAD_X0687_N_L
GAC_W0451_N_E
HCC_G0213_T_L
HCC_G0218_N_L
-   Mapping and Sequencing
Base Position
p14 Fix Patches
p14 Alt Haplotypes
Assembly
Assembly Tracks
Centromeres
Chromosome Band
Clone Ends
Exome Probesets
Gap
GC Percent
GRC Incident
Hg19 Diff
INSDC
LiftOver & ReMap
LRG Regions
Mappability
updated Problematic Regions
Recomb Rate
RefSeq Acc
Restr Enzymes
Short Match
-   Genes and Gene Predictions
updated GENCODE V47
NCBI RefSeq
CCDS
CRISPR Targets
GENCODE Archive
updated GENCODE Versions
HGNC
IKMC Genes Mapped
LRG Transcripts
MANE
MGC/ORFeome Genes
Non-coding RNA
Old UCSC Genes
Other RefSeq
Pfam in GENCODE
Prediction Archive
RetroGenes V9
TransMap V5
UCSC Alt Events
UniProt
-   Phenotype and Literature
OMIM
AbSplice Scores
CADD 1.6
new CADD 1.7
Cancer Gene Expr
new ClinGen
ClinGen CNVs
ClinVar Variants
Constraint scores
Coriell CNVs
COSMIC
COSMIC Regions
COVID Data
DECIPHER CNVs
DECIPHER SNVs
Development Delay
Dosage Sensitivity
GenCC
Gene Interactions
GeneReviews
GWAS Catalog
HGMD public
LOVD Variants
Orphanet
PanelApp
REVEL Scores
SNPedia
new SpliceAI
TCGA Pan-Cancer
UniProt Variants
Variants in Papers
-   Human Pangenome - HPRC
Multiple Alignment
Pairwise Alignments
Rearrangements
Short Variants
-   mRNA and EST
Human ESTs
Human mRNAs
Other ESTs
Other mRNAs
SIB Alt-Splicing
Spliced ESTs
-   Expression
GTEx Gene V8
GTEx RNA-Seq Coverage
Affy Archive
EPDnew Promoters
GNF Atlas 2
GTEx Gene
GTEx Transcript
GWIPS-viz Riboseq
miRNA Tissue Atlas
Single Cell Expression
+   Single Cell RNA-seq
-   Regulation
ENCODE cCREs
ENCODE Regulation
CpG Islands
FANTOM5
GeneHancer
GTEx cis-eQTLs
Hi-C and Micro-C
JASPAR Transcription Factors
ORegAnno
RefSeq Func Elems
ReMap ChIP-seq
VISTA Enhancers
-   Comparative Genomics
Conservation
Cactus 241-way
Cons 30 Primates
Primate Chain/Net
Placental Chain/Net
Vertebrate Chain/Net
Cactus 447-way
CHM13 alignments
Multiz 470-way
-   Variation
dbSNP 155
1000 Genomes
Array Probesets
dbSNP Archive
dbVar Common Struct Var
DGV Struct Var
Genome In a Bottle
new gnomAD Variants
Platinum Genomes
-   Repeats
RepeatMasker
Interrupted Rpts
Microsatellite
NuMTs Sequence
RepeatMasker Viz.
Segmental Dups
Self Alignment
Simple Repeats
WM + SDust
Invisible link