Variant report

Variant rs4668308
Chromosome Location chr2:171600018-171600019
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171574000-171620800 Weak transcription Pancreas Pancrea
2 chr2:171593600-171600800 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr2:171594000-171600200 Weak transcription Primary monocytes fromperipheralblood blood
4 chr2:171595200-171600200 Weak transcription Gastric stomach
5 chr2:171596200-171600200 Enhancers K562 blood
6 chr2:171596200-171601200 Weak transcription HSMMtube muscle
7 chr2:171597600-171603800 Weak transcription HMEC breast
8 chr2:171597800-171604000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:171598000-171603800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr2:171598400-171600600 Enhancers Fetal Intestine Small intestine
11 chr2:171599800-171600400 Enhancers HepG2 liver
12 chr2:171599800-171601800 Enhancers Stomach Mucosa stomach
13 chr2:171600000-171600200 Enhancers Fetal Intestine Large intestine
14 chr2:171600000-171600600 Weak transcription Duodenum Mucosa Duodenum

Quick Search:


  
Input of quick search could be:

what's new

Quick links