Variant report

Variant rs28559568
Chromosome Location chr15:45407967-45407968
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:45406000-45410800 Bivalent Enhancer Stomach Mucosa stomach
2 chr15:45406600-45410200 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
3 chr15:45406600-45410400 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
4 chr15:45406800-45408000 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
5 chr15:45406800-45408800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
6 chr15:45407000-45408600 Bivalent Enhancer Primary T helper naive cells fromperipheralblood blood
7 chr15:45407000-45408800 Weak transcription Pancreas Pancrea
8 chr15:45407400-45408600 Weak transcription Gastric stomach
9 chr15:45407600-45408000 Bivalent Enhancer Colonic Mucosa Colon
10 chr15:45407800-45408200 Bivalent Enhancer Right Ventricle heart

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