Variant report

Variant rs62169548
Chromosome Location chr2:171591351-171591352
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171574000-171620800 Weak transcription Pancreas Pancrea
2 chr2:171586400-171592200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr2:171590000-171591600 Enhancers NHEK skin
4 chr2:171590200-171591400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr2:171590200-171591600 Enhancers Placenta Placenta
6 chr2:171590400-171591400 Enhancers Fetal Intestine Large intestine
7 chr2:171590400-171591600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr2:171590400-171591600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr2:171590400-171591600 Enhancers Fetal Intestine Small intestine
10 chr2:171590600-171591400 Enhancers HepG2 liver
11 chr2:171591000-171591600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr2:171591200-171594200 Weak transcription HMEC breast

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