The 2.0 version of rSNPBase

Variant report

Variant rs788855
Chromosome Location chr4:82128630-82128631
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:82122200-82129400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr4:82125400-82130600 Enhancers Fetal Intestine Large intestine
3 chr4:82126400-82130800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr4:82126800-82134800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
5 chr4:82127800-82129600 Enhancers Fetal Intestine Small intestine
6 chr4:82127800-82130400 Enhancers NHDF-Ad bronchial
7 chr4:82127800-82130800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr4:82128000-82130200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr4:82128000-82130600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr4:82128400-82129600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr4:82128400-82129800 Enhancers NHLF lung
12 chr4:82128600-82129000 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr4:82128600-82129400 Enhancers Primary neutrophils fromperipheralblood blood
14 chr4:82128600-82129600 Enhancers Muscle Satellite Cultured Cells --
15 chr4:82128600-82129800 Enhancers HMEC breast

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Last update: Aug 31, 2015