Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:200811324-200811572 | Common:1; Rare:77 | ||||
chr2:200889073-200889424 | Common:2; Rare:115 | ||||
chr2:201071616-201072012 | Rare:81 | ||||
chr2:201451542-201451814 | Common:2; Rare:74 | ||||
chr2:201642643-201642773 | Rare:66 | ||||
chr2:201643444-201643553 | Rare:31; Clinvar:3 | ||||
chr2:202912147-202912286 | Common:1; Rare:50 | ||||
chr2:203238827-203239054 | Common:1; Rare:89 | ||||
chr2:203239229-203239344 | Rare:40 | ||||
chr2:203535307-203535581 | Common:3; Rare:130 | ||||
chr2:206159410-206159987 | Common:1; Rare:172 | ||||
chr2:206274917-206275043 | Rare:47 | ||||
chr2:206765297-206765615 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
chr2:207529774-207530102 | Common:3; Rare:93 | ||||
chr2:208025503-208025618 | Rare:29 |