The 2.0 version of rSNPBase

Variant report

Variant rs6948617
Chromosome Location chr7:19062430-19062431
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:19056000-19063600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr7:19060600-19064000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr7:19060800-19063600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr7:19061000-19063200 Weak transcription Osteobl bone
5 chr7:19061000-19063400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr7:19061000-19063400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr7:19061000-19063600 Weak transcription Muscle Satellite Cultured Cells --
8 chr7:19061000-19063800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr7:19061200-19063400 Weak transcription NHDF-Ad bronchial
10 chr7:19061200-19063600 Weak transcription NH-A brain
11 chr7:19061200-19064000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr7:19061400-19063400 Weak transcription NHEK skin
13 chr7:19061400-19065800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr7:19061600-19063200 Weak transcription HSMM muscle
15 chr7:19061600-19064000 Weak transcription HMEC breast

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Last update: Aug 31, 2015