Variant report

Variant rs2907585
Chromosome Location chr10:117614128-117614129
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:117607600-117621400 Weak transcription Aorta Aorta
2 chr10:117609400-117614200 Weak transcription Muscle Satellite Cultured Cells --
3 chr10:117612200-117616600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr10:117612200-117628000 Weak transcription Ovary ovary
5 chr10:117613800-117614200 Enhancers Pancreas Pancrea
6 chr10:117613800-117614600 Enhancers Esophagus oesophagus
7 chr10:117613800-117614800 Enhancers Placenta Amnion Placenta Amnion
8 chr10:117613800-117615000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr10:117613800-117615000 Flanking Active TSS NHEK skin
10 chr10:117614000-117614200 Enhancers H9 Cell Line embryonic stem cell
11 chr10:117614000-117614200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
12 chr10:117614000-117614600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr10:117614000-117614600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr10:117614000-117614800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr10:117614000-117615000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr10:117614000-117615200 Enhancers HMEC breast

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