Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:32970611-32970959 | Common:2; Rare:90 | ||||
chr6:32977530-32977909 | Common:3; Rare:126; Clinvar (benign):1 | ||||
chr6:33075795-33076071 | Common:4; Rare:38 | ||||
chr6:33200356-33200454 | Rare:26 | ||||
chr6:33200654-33200938 | Common:2; Rare:85 | ||||
chr6:33202101-33202379 | Common:3; Rare:88 | ||||
chr6:33208308-33208524 | Common:1; Rare:50 | ||||
chr6:33271653-33272122 | Common:2; Rare:166 | ||||
chr6:33276904-33277405 | Common:3; Rare:168 | ||||
chr6:33288970-33289125 | Rare:60 | ||||
chr6:33289186-33289383 | Common:1; Rare:50 | ||||
chr6:33296437-33296695 | Common:1; Rare:67 | ||||
chr6:33298905-33299064 | Rare:42 | ||||
chr6:33299408-33299518 | Common:1; Rare:26 | ||||
chr6:33322912-33323265 | Common:5; Rare:107 |