Variant report

Variant rs9297782
Chromosome Location chr8:130047294-130047295
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:130036400-130051000 Weak transcription Fetal Thymus thymus
2 chr8:130042800-130047400 Weak transcription Right Atrium heart
3 chr8:130045400-130048000 Strong transcription Dnd41 blood
4 chr8:130046800-130047400 Enhancers Muscle Satellite Cultured Cells --
5 chr8:130046800-130047800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr8:130046800-130047800 Enhancers Skeletal Muscle Female skeletal muscle
7 chr8:130046800-130047800 Enhancers NHEK skin
8 chr8:130047000-130047400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr8:130047000-130047600 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr8:130047000-130047600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
11 chr8:130047000-130047600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr8:130047000-130047800 Enhancers HMEC breast
13 chr8:130047200-130047600 Enhancers A549 lung
14 chr8:130047200-130047800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr8:130047200-130048000 Enhancers HUES6 Cell Line embryonic stem cell

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