Variant report

Variant rs9997709
Chromosome Location chr4:81133944-81133945
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:81124800-81134200 Weak transcription NHLF lung
2 chr4:81124800-81135200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr4:81125000-81134200 Weak transcription NHDF-Ad bronchial
4 chr4:81126400-81134200 Weak transcription HSMM muscle
5 chr4:81128600-81134200 Weak transcription HMEC breast
6 chr4:81128800-81134400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr4:81129000-81134400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr4:81129600-81134600 Weak transcription Gastric stomach
9 chr4:81130000-81134400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr4:81132600-81134400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr4:81132800-81134000 Weak transcription NHEK skin
12 chr4:81133400-81135400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr4:81133600-81135200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr4:81133800-81134200 Weak transcription Fetal Heart heart
15 chr4:81133800-81134200 Weak transcription K562 blood

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