Variant report

Variant rs191769288
Chromosome Location chr10:23477800-23477801
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:23476600-23478600 Bivalent Enhancer HepG2 liver
2 chr10:23477000-23477800 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
3 chr10:23477600-23478200 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
4 chr10:23477600-23478200 Flanking Active TSS Pancreas Pancrea
5 chr10:23477600-23478400 Bivalent Enhancer H1 Cell Line embryonic stem cell
6 chr10:23477800-23478000 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
7 chr10:23477800-23478000 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
8 chr10:23477800-23478200 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
9 chr10:23477800-23478600 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
10 chr10:23477800-23478600 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell

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