The 2.0 version of rSNPBase

Variant report

Variant rs710838
Chromosome Location chr4:82133243-82133244
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:82126800-82134800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr4:82130400-82133600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr4:82130600-82133600 Weak transcription Fetal Brain Male brain
4 chr4:82131800-82133600 Weak transcription Fetal Intestine Small intestine
5 chr4:82132000-82135000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr4:82132200-82136200 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr4:82132600-82133400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr4:82132800-82133600 Enhancers NHDF-Ad bronchial
9 chr4:82132800-82133800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr4:82132800-82134000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr4:82132800-82135400 Active TSS Fetal Intestine Large intestine
12 chr4:82133000-82133600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr4:82133200-82133400 Enhancers Right Atrium heart
14 chr4:82133200-82133400 Enhancers NHLF lung
15 chr4:82133200-82136000 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Female --

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Last update: Aug 31, 2015