Variant report

Variant rs357053
Chromosome Location chr1:180230872-180230873
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:180222600-180239200 Weak transcription Gastric stomach
2 chr1:180223800-180234400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr1:180224000-180234400 Weak transcription ES-WA7 Cell Line embryonic stem cell
4 chr1:180224600-180234200 Weak transcription H1 Cell Line embryonic stem cell
5 chr1:180229400-180234000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr1:180229400-180240400 Weak transcription Right Atrium heart
7 chr1:180229800-180232800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr1:180230200-180231000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr1:180230600-180231000 Enhancers Pancreatic Islets Pancreatic Islet
10 chr1:180230600-180232200 Bivalent Enhancer Fetal Stomach stomach
11 chr1:180230800-180231000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
12 chr1:180230800-180231000 Bivalent Enhancer Fetal Muscle Trunk muscle
13 chr1:180230800-180231000 Enhancers HSMMtube muscle
14 chr1:180230800-180231200 Bivalent Enhancer IMR90 fetal lung fibroblasts Cell Line lung
15 chr1:180230800-180232000 Weak transcription Pancreas Pancrea
16 chr1:180230800-180232200 Enhancers Breast Myoepithelial Primary Cells Breast
17 chr1:180230800-180232200 Enhancers Colon Smooth Muscle Colon

Quick Search:


  
Input of quick search could be:

what's new

Quick links