Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:46860778-46861134 | Common:3; Rare:114 | ||||
chr19:47243115-47243402 | Common:4; Rare:66 | ||||
chr19:48397683-48397749 | Common:1; Rare:15 | ||||
chr2:11102764-11102962 | Rare:35 | ||||
chr2:20037422-20037592 | Rare:40 | ||||
chr2:28301022-28301326 | Common:1; Rare:52 | ||||
chr2:32916262-32916349 | |||||
chr2:36539480-36539682 | Rare:50 | ||||
chr2:36564467-36564607 | Common:1; Rare:33 | ||||
chr2:47162393-47162565 | Rare:43; Clinvar (benign):2 | ||||
chr2:47175155-47175250 | Common:1; Rare:23 | ||||
chr2:47803162-47803493 | Common:2; Rare:122; Clinvar:22; Clinvar (benign):15 | ||||
chr2:62881164-62881262 | Common:1; Rare:13 | ||||
chr2:65436528-65436744 | Rare:57 | ||||
chr2:67398093-67398159 | Rare:13 |