Variant report

Variant rs1629253
Chromosome Location chr19:39537296-39537297
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:39530800-39543000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr19:39535400-39538800 Enhancers Fetal Intestine Large intestine
3 chr19:39535400-39538800 Enhancers Fetal Intestine Small intestine
4 chr19:39535800-39538800 Enhancers Duodenum Mucosa Duodenum
5 chr19:39536400-39537400 Flanking Active TSS K562 blood
6 chr19:39536400-39538200 Enhancers Stomach Mucosa stomach
7 chr19:39536600-39537400 Enhancers GM12878-XiMat blood
8 chr19:39536600-39537600 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr19:39536800-39537400 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
10 chr19:39537000-39537600 Enhancers A549 lung
11 chr19:39537200-39541800 Weak transcription HepG2 liver

Quick Search:


  
Input of quick search could be:

what's new

Quick links