The 2.0 version of rSNPBase

Variant report

Variant rs7662417
Chromosome Location chr4:81217404-81217405
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:81190600-81223800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr4:81202200-81226200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr4:81206800-81222800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr4:81210000-81225800 Weak transcription Muscle Satellite Cultured Cells --
5 chr4:81210400-81226200 Weak transcription HSMM muscle
6 chr4:81211400-81226200 Weak transcription NH-A brain
7 chr4:81213200-81218000 Genic enhancers Osteobl bone
8 chr4:81214200-81217600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr4:81214600-81217600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr4:81215600-81217800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr4:81216200-81218000 Enhancers NHLF lung
12 chr4:81216400-81217600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr4:81217400-81223000 Weak transcription NHDF-Ad bronchial

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Last update: Aug 31, 2015