Variant report

Variant rs17501857
Chromosome Location chr7:27286538-27286539
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:27283600-27293600 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
2 chr7:27284200-27286800 Bivalent Enhancer Lung lung
3 chr7:27285600-27286800 Bivalent Enhancer H1 Cell Line embryonic stem cell
4 chr7:27286000-27286600 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
5 chr7:27286000-27287200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
6 chr7:27286000-27291200 Weak transcription Gastric stomach
7 chr7:27286200-27286600 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell
8 chr7:27286200-27286600 Bivalent Enhancer Right Ventricle heart
9 chr7:27286200-27286800 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
10 chr7:27286200-27287000 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr7:27286200-27287000 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
12 chr7:27286200-27291000 Weak transcription Right Atrium heart
13 chr7:27286200-27291200 Weak transcription Pancreas Pancrea
14 chr7:27286400-27286600 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links