Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:31739751-31740012 | Common:2; Rare:58 | ||||
chr6:31827467-31827746 | Common:2; Rare:84 | ||||
chr6:31827910-31827933 | Common:1; Rare:15 | ||||
chr6:31834660-31834922 | Common:3; Rare:54 | ||||
chr6:31897670-31897782 | Rare:21 | ||||
chr6:31958899-31959204 | Rare:101; Clinvar:8 | ||||
chr6:32109275-32109376 | Rare:21 | ||||
chr6:32176079-32176293 | Common:1; Rare:42 | ||||
chr6:32178092-32178458 | Common:2; Rare:54 | ||||
chr6:32190171-32190422 | Rare:41 | ||||
chr6:32666652-32666875 | Common:31; Rare:22 | ||||
chr6:32844002-32844105 | Rare:24; Clinvar:1 | ||||
chr6:32844631-32844848 | Common:1; Rare:48 | ||||
chr6:32853680-32853884 | Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
chr6:32854024-32854204 | Common:2; Rare:47 |