Variant report

Variant rs10185519
Chromosome Location chr2:171597459-171597460
allele C/G
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 chr2:171593200-171598000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr2:171593600-171600800 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr2:171594000-171600200 Weak transcription Primary monocytes fromperipheralblood blood
5 chr2:171594200-171597600 Enhancers HMEC breast
6 chr2:171595000-171597800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr2:171595200-171600200 Weak transcription Gastric stomach
8 chr2:171596000-171598000 Enhancers NHEK skin
9 chr2:171596200-171600200 Enhancers K562 blood
10 chr2:171596200-171601200 Weak transcription HSMMtube muscle
11 chr2:171596400-171599200 Weak transcription NH-A brain
12 chr2:171596600-171598400 Weak transcription Fetal Intestine Small intestine
13 chr2:171596800-171598200 Weak transcription Fetal Intestine Large intestine
14 chr2:171596800-171599800 Weak transcription Stomach Mucosa stomach
15 chr2:171597200-171597600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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