Variant report

Variant rs11096639
Chromosome Location chr2:20305429-20305430
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:20298400-20307800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:20301200-20306400 Weak transcription HUVEC blood vessel
3 chr2:20303400-20306400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr2:20303600-20307000 Enhancers Esophagus oesophagus
5 chr2:20304000-20306200 Weak transcription HMEC breast
6 chr2:20304200-20306000 Enhancers Stomach Mucosa stomach
7 chr2:20304600-20305800 Enhancers Placenta Placenta
8 chr2:20304600-20306800 Weak transcription Fetal Lung lung
9 chr2:20304800-20305600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr2:20304800-20306400 Weak transcription Pancreas Pancrea
11 chr2:20304800-20308600 Weak transcription Liver Liver
12 chr2:20305000-20306400 Weak transcription Spleen Spleen
13 chr2:20305200-20307200 Weak transcription HepG2 liver
14 chr2:20305200-20308600 Weak transcription Rectal Mucosa Donor 31 rectum
15 chr2:20305400-20305600 Weak transcription Gastric stomach
16 chr2:20305400-20306400 Weak transcription Lung lung

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