The 2.0 version of rSNPBase

Variant report

Variant rs12066755
Chromosome Location chr1:215231442-215231443
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:215222800-215242200 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr1:215228000-215233400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr1:215228000-215237200 Weak transcription Pancreas Pancrea
4 chr1:215228600-215231600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr1:215228800-215231600 Enhancers NHDF-Ad bronchial
6 chr1:215229000-215233800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr1:215229200-215237800 Weak transcription NHEK skin
8 chr1:215229400-215231800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr1:215229400-215253000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr1:215230600-215232200 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr1:215231200-215232000 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr1:215231400-215231800 Enhancers H9 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links

Copyright © 2015, Bioinformatics Lab, Institute of Psychology, Chinese Academy of Sciences. All Rights Reserved Feedback
Last update: Aug 31, 2015