Variant report

Variant rs7089767
Chromosome Location chr10:119236737-119236738
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:119223200-119237400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr10:119235200-119238200 Enhancers Colon Smooth Muscle Colon
3 chr10:119235600-119238200 Enhancers Rectal Smooth Muscle rectum
4 chr10:119235800-119237400 Enhancers Fetal Muscle Leg muscle
5 chr10:119235800-119238400 Enhancers Osteobl bone
6 chr10:119236400-119236800 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr10:119236400-119236800 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr10:119236400-119236800 Enhancers HUVEC blood vessel
9 chr10:119236400-119236800 Flanking Active TSS NHDF-Ad bronchial
10 chr10:119236400-119237000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
11 chr10:119236400-119237200 Enhancers HMEC breast
12 chr10:119236400-119237400 Enhancers Fetal Muscle Trunk muscle
13 chr10:119236400-119237600 Enhancers Adipose Nuclei Adipose
14 chr10:119236600-119238000 Enhancers Skeletal Muscle Male skeletal muscle
15 chr10:119236600-119238400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin

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