Variant report

Variant rs7582102
Chromosome Location chr2:171590668-171590669
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr2:171586800-171590800 Weak transcription HMEC breast
4 chr2:171590000-171591600 Enhancers NHEK skin
5 chr2:171590200-171591000 Enhancers Duodenum Mucosa Duodenum
6 chr2:171590200-171591400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr2:171590200-171591600 Enhancers Placenta Placenta
8 chr2:171590400-171591000 Enhancers K562 blood
9 chr2:171590400-171591400 Enhancers Fetal Intestine Large intestine
10 chr2:171590400-171591600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr2:171590400-171591600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr2:171590400-171591600 Enhancers Fetal Intestine Small intestine
13 chr2:171590600-171591000 Genic enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr2:171590600-171591000 Enhancers HSMMtube muscle
15 chr2:171590600-171591400 Enhancers HepG2 liver

Quick Search:


  
Input of quick search could be:

what's new

Quick links