Variant report

Variant rs7029338
Chromosome Location chr9:140780836-140780837
allele C/T
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 chr9:140777200-140782000 ZNF genes & repeats Spleen Spleen
3 chr9:140777600-140787200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
4 chr9:140778600-140787000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr9:140779200-140785000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr9:140780200-140781000 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin02 Skin
7 chr9:140780400-140781000 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr9:140780600-140781600 Bivalent/Poised TSS H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr9:140780600-140782400 Genic enhancers Brain Germinal Matrix brain
10 chr9:140780600-140783400 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
11 chr9:140780800-140782000 Strong transcription iPS-15b Cell Line embryonic stem cell

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