The 2.0 version of rSNPBase

Variant report

Variant rs4647398
Chromosome Location chr9:98048575-98048576
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:98045400-98048800 Enhancers Fetal Intestine Large intestine
2 chr9:98045800-98048800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr9:98046200-98050200 Enhancers Liver Liver
4 chr9:98046600-98048800 Weak transcription Small Intestine intestine
5 chr9:98046600-98059400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr9:98046600-98063000 Weak transcription Fetal Stomach stomach
7 chr9:98047000-98048800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr9:98047200-98059400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr9:98047400-98055800 Weak transcription HepG2 liver
10 chr9:98048000-98055000 Weak transcription Fetal Intestine Small intestine
11 chr9:98048200-98048600 Weak transcription NHLF lung
12 chr9:98048200-98048800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr9:98048200-98048800 Enhancers Pancreatic Islets Pancreatic Islet
14 chr9:98048200-98049000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr9:98048200-98050200 Enhancers A549 lung

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Last update: Aug 31, 2015