Variant report

Variant rs35813830
Chromosome Location chr12:76077791-76077792
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:76076200-76098400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr12:76076600-76079800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr12:76076800-76080000 Enhancers NHEK skin
4 chr12:76077000-76078200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
5 chr12:76077000-76079400 Enhancers Fetal Stomach stomach
6 chr12:76077000-76079600 Enhancers HMEC breast
7 chr12:76077000-76081800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr12:76077200-76078000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr12:76077200-76078200 Enhancers Osteobl bone
10 chr12:76077200-76078400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr12:76077200-76079200 Enhancers K562 blood
12 chr12:76077200-76079800 Enhancers NHLF lung
13 chr12:76077400-76078400 Enhancers NHDF-Ad bronchial
14 chr12:76077600-76079800 Enhancers NH-A brain

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