The 2.0 version of rSNPBase

Variant report

Variant rs66517241
Chromosome Location chr4:22364812-22364813
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:22329000-22389400 Weak transcription Pancreas Pancrea
2 chr4:22336600-22385400 Weak transcription Fetal Intestine Large intestine
3 chr4:22354000-22378200 Weak transcription Aorta Aorta
4 chr4:22359000-22365000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr4:22362400-22366400 Weak transcription Ovary ovary
6 chr4:22364000-22365600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr4:22364000-22365800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr4:22364000-22366000 Enhancers NHEK skin
9 chr4:22364000-22366200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr4:22364000-22366400 Enhancers Muscle Satellite Cultured Cells --
11 chr4:22364200-22366000 Enhancers HMEC breast
12 chr4:22364400-22365200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
13 chr4:22364400-22366600 Enhancers Osteobl bone
14 chr4:22364800-22366400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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Last update: Aug 31, 2015