Variant report

Variant rs562511069
Chromosome Location chr19:55873916-55873917
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:55866200-55880600 Weak transcription Right Atrium heart
2 chr19:55869800-55874000 Weak transcription Placenta Amnion Placenta Amnion
3 chr19:55871400-55877000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr19:55871400-55880200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr19:55871800-55874200 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr19:55872000-55874000 Weak transcription H1 Cell Line embryonic stem cell
7 chr19:55873400-55879800 Weak transcription HSMM muscle
8 chr19:55873600-55874200 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
9 chr19:55873600-55874400 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
10 chr19:55873600-55874600 Enhancers ES-WA7 Cell Line embryonic stem cell
11 chr19:55873600-55874600 Bivalent/Poised TSS Foreskin Melanocyte Primary Cells skin01 Skin
12 chr19:55873600-55875200 Enhancers Placenta Placenta
13 chr19:55873600-55876200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr19:55873800-55874000 Weak transcription HUES6 Cell Line embryonic stem cell
15 chr19:55873800-55874000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin

Quick Search:


  
Input of quick search could be:

what's new

Quick links