Variant report

Variant rs34859525
Chromosome Location chr9:140783921-140783922
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 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 chr9:140782000-140785400 Weak transcription iPS-15b Cell Line embryonic stem cell
6 chr9:140782400-140784000 Strong transcription Brain Germinal Matrix brain
7 chr9:140783200-140784200 Enhancers Fetal Thymus thymus
8 chr9:140783200-140785600 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
9 chr9:140783600-140784000 ZNF genes & repeats Spleen Spleen
10 chr9:140783600-140785200 Bivalent Enhancer Fetal Brain Female brain
11 chr9:140783800-140785600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell

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