The 2.0 version of rSNPBase

Variant report

Variant rs35166938
Chromosome Location chr4:81213780-81213781
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr4:81200000-81216600 Weak transcription HMEC breast
3 chr4:81202200-81226200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr4:81206800-81222800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr4:81208000-81216200 Weak transcription NHLF lung
6 chr4:81209000-81215000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr4:81210000-81214000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr4:81210000-81225800 Weak transcription Muscle Satellite Cultured Cells --
9 chr4:81210400-81226200 Weak transcription HSMM muscle
10 chr4:81211400-81226200 Weak transcription NH-A brain
11 chr4:81212000-81214200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr4:81212000-81214600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
13 chr4:81212000-81215400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr4:81213200-81218000 Genic enhancers Osteobl bone
15 chr4:81213400-81215000 Genic enhancers NHDF-Ad bronchial

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Last update: Aug 31, 2015