Variant report

Variant rs10817632
Chromosome Location chr9:117270853-117270854
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:117268600-117274000 Weak transcription Rectal Mucosa Donor 31 rectum
2 chr9:117268600-117275400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr9:117269800-117271000 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
4 chr9:117269800-117271200 Enhancers ES-I3 Cell Line embryonic stem cell
5 chr9:117270000-117271000 Bivalent Enhancer Fetal Thymus thymus
6 chr9:117270000-117271200 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr9:117270000-117271400 Enhancers H1 Cell Line embryonic stem cell
8 chr9:117270000-117274400 Weak transcription Duodenum Mucosa Duodenum
9 chr9:117270200-117271400 Enhancers HUES48 Cell Line embryonic stem cell
10 chr9:117270400-117273800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr9:117270600-117271400 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr9:117270600-117275000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
13 chr9:117270800-117271000 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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