Variant report

Variant rs9989105
Chromosome Location chr13:110691233-110691234
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:110682200-110694600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr13:110687400-110696800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr13:110689200-110695600 Weak transcription H9 Cell Line embryonic stem cell
4 chr13:110689200-110695600 Weak transcription Gastric stomach
5 chr13:110689200-110696800 Weak transcription ES-I3 Cell Line embryonic stem cell
6 chr13:110689200-110700200 Weak transcription Right Atrium heart
7 chr13:110689400-110695600 Weak transcription Aorta Aorta
8 chr13:110689400-110695800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr13:110689600-110694800 Weak transcription Cortex derived primary cultured neurospheres brain
10 chr13:110690000-110691400 Enhancers Dnd41 blood
11 chr13:110690000-110691600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr13:110690600-110691800 ZNF genes & repeats Ganglion Eminence derived primary cultured neurospheres brain

Quick Search:


  
Input of quick search could be:

what's new

Quick links