Variant report

Variant rs2067056
Chromosome Location chr9:104501567-104501568
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:104499400-104501600 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
2 chr9:104500000-104501600 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
3 chr9:104501000-104501800 Enhancers Pancreas Pancrea
4 chr9:104501200-104501600 Bivalent Enhancer ES-WA7 Cell Line embryonic stem cell
5 chr9:104501200-104501600 Enhancers Fetal Stomach stomach
6 chr9:104501200-104502400 Bivalent Enhancer H1 Cell Line embryonic stem cell
7 chr9:104501400-104501600 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
8 chr9:104501400-104501600 Flanking Bivalent TSS/Enh iPS-20b Cell Line embryonic stem cell
9 chr9:104501400-104502200 Enhancers Ovary ovary
10 chr9:104501400-104502400 Flanking Bivalent TSS/Enh HUES48 Cell Line embryonic stem cell
11 chr9:104501400-104502600 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
12 chr9:104501400-104502800 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell

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