Variant report

Variant rs2508254
Chromosome Location chr11:101489573-101489574
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:101481200-101489800 Weak transcription ES-WA7 Cell Line embryonic stem cell
2 chr11:101487200-101490400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr11:101487800-101490000 Enhancers HMEC breast
4 chr11:101488200-101489800 Enhancers NHDF-Ad bronchial
5 chr11:101488200-101490000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr11:101488200-101490400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr11:101488400-101490000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr11:101488600-101489600 Enhancers NH-A brain
9 chr11:101488600-101490000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr11:101489000-101489600 Enhancers Muscle Satellite Cultured Cells --
11 chr11:101489200-101489600 Flanking Active TSS NHEK skin
12 chr11:101489400-101490000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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