Variant report

Variant rs555819586
Chromosome Location chr9:71927971-71927972
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:71926200-71931800 Weak transcription Fetal Heart heart
2 chr9:71926400-71929800 ZNF genes & repeats H1 Cell Line embryonic stem cell
3 chr9:71927000-71929200 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
4 chr9:71927000-71929600 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
5 chr9:71927400-71928200 ZNF genes & repeats HUES48 Cell Line embryonic stem cell
6 chr9:71927600-71928000 ZNF genes & repeats hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr9:71927600-71928000 ZNF genes & repeats iPS DF 6.9 Cell Line embryonic stem cell
8 chr9:71927600-71928400 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr9:71927600-71928400 ZNF genes & repeats Aorta Aorta

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