Variant report

Variant rs529014016
Chromosome Location chr9:140783728-140783729
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:140773200-140795400 Weak transcription Right Atrium heart
2 chr9:140777600-140787200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
3 chr9:140778600-140787000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr9:140779200-140785000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr9:140781600-140783800 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr9:140782000-140785400 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr9:140782400-140784000 Strong transcription Brain Germinal Matrix brain
8 chr9:140783200-140784200 Enhancers Fetal Thymus thymus
9 chr9:140783200-140785600 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
10 chr9:140783400-140783800 Transcr. at gene 5' and 3' iPS DF 19.11 Cell Line embryonic stem cell
11 chr9:140783400-140783800 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
12 chr9:140783600-140783800 Bivalent Enhancer Brain Dorsolateral Prefrontal Cortex brain
13 chr9:140783600-140783800 Bivalent Enhancer HMEC breast
14 chr9:140783600-140784000 ZNF genes & repeats Spleen Spleen
15 chr9:140783600-140785200 Bivalent Enhancer Fetal Brain Female brain

Quick Search:


  
Input of quick search could be:

what's new

Quick links