Variant report

Variant rs542088062
Chromosome Location chr9:17578136-17578137
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:4 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:17577800-17578200 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
2 chr9:17577800-17578200 Active TSS Spleen Spleen
3 chr9:17577800-17580000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
4 chr9:17578000-17578200 Bivalent/Poised TSS Fetal Intestine Small intestine

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