Variant report

Variant rs7895619
Chromosome Location chr10:4764644-4764645
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:4749200-4769400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr10:4760400-4767800 Weak transcription Rectal Smooth Muscle rectum
3 chr10:4762200-4765600 Weak transcription Muscle Satellite Cultured Cells --
4 chr10:4762400-4768800 Enhancers NHDF-Ad bronchial
5 chr10:4762600-4767200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr10:4763000-4766000 Weak transcription A549 lung
7 chr10:4763400-4765200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
8 chr10:4763600-4766400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr10:4763800-4765400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr10:4763800-4765600 Enhancers NHLF lung
11 chr10:4764200-4764800 Enhancers Osteobl bone
12 chr10:4764400-4767400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr10:4764400-4767800 Weak transcription NH-A brain
14 chr10:4764400-4768400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
15 chr10:4764600-4764800 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr10:4764600-4765200 Weak transcription HMEC breast

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