Variant report

Variant rs7995717
Chromosome Location chr13:80016086-80016087
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:80010200-80025600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr13:80015200-80016200 Enhancers HUES6 Cell Line embryonic stem cell
3 chr13:80015400-80016200 Enhancers H1 Cell Line embryonic stem cell
4 chr13:80015400-80016200 Enhancers HUES48 Cell Line embryonic stem cell
5 chr13:80015400-80016200 Enhancers iPS-18 Cell Line embryonic stem cell
6 chr13:80015400-80020200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr13:80015600-80016400 Enhancers Pancreas Pancrea
8 chr13:80015600-80017000 Active TSS Rectal Mucosa Donor 29 rectum
9 chr13:80015800-80016200 Enhancers Colonic Mucosa Colon
10 chr13:80015800-80016400 Enhancers Duodenum Mucosa Duodenum
11 chr13:80015800-80016400 Enhancers Rectal Mucosa Donor 31 rectum
12 chr13:80016000-80016400 Flanking Active TSS A549 lung
13 chr13:80016000-80016400 Flanking Active TSS HepG2 liver
14 chr13:80016000-80016800 ZNF genes & repeats Fetal Intestine Large intestine
15 chr13:80016000-80017200 Enhancers Stomach Mucosa stomach
16 chr13:80016000-80019600 Weak transcription ES-I3 Cell Line embryonic stem cell

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