Variant report

Variant rs62168366
Chromosome Location chr2:171595040-171595041
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171574000-171620800 Weak transcription Pancreas Pancrea
2 chr2:171591400-171595200 Weak transcription Fetal Intestine Large intestine
3 chr2:171591600-171595200 Weak transcription Placenta Placenta
4 chr2:171593200-171598000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr2:171593600-171595200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr2:171593600-171600800 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr2:171593800-171595400 Enhancers NHEK skin
8 chr2:171594000-171597200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:171594000-171600200 Weak transcription Primary monocytes fromperipheralblood blood
10 chr2:171594200-171596800 Enhancers Stomach Mucosa stomach
11 chr2:171594200-171597600 Enhancers HMEC breast
12 chr2:171594400-171595600 Enhancers Muscle Satellite Cultured Cells --
13 chr2:171594400-171596400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
14 chr2:171594400-171596400 Enhancers HSMM muscle
15 chr2:171594400-171596600 Enhancers Fetal Intestine Small intestine
16 chr2:171594400-171597400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr2:171594600-171595200 Weak transcription NH-A brain
18 chr2:171594600-171596600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
19 chr2:171595000-171597800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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