Variant report

Variant rs4667654
Chromosome Location chr2:171599590-171599591
allele G/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 chr2:171593600-171600800 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 chr2:171596800-171599800 Weak transcription Stomach Mucosa stomach
8 chr2:171597600-171603800 Weak transcription HMEC breast
9 chr2:171597800-171604000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:171598000-171603800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr2:171598400-171600600 Enhancers Fetal Intestine Small intestine
12 chr2:171599000-171600000 Weak transcription Fetal Intestine Large intestine

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