Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:57867922-57868062 | Rare:28 | ||||
chr19:58230265-58230465 | Common:1; Rare:37 | ||||
chr19:58249606-58249646 | Rare:5 | ||||
chr19:58575361-58575587 | Rare:57 | ||||
chr19:58575665-58575778 | Rare:20 | ||||
chr2:226680-226967 | Common:6; Rare:45 | ||||
chr2:232585-232864 | Common:1; Rare:44 | ||||
chr2:276859-277030 | Common:4; Rare:32; Clinvar (benign):1 | ||||
chr2:277045-277231 | Common:2; Rare:42 | ||||
chr2:1052939-1053182 | Common:6; Rare:37 | ||||
chr2:1631720-1631898 | Rare:26 | ||||
chr2:1656478-1656589 | Rare:27 | ||||
chr2:3514805-3515090 | Common:2; Rare:64 | ||||
chr2:3536479-3536658 | Common:2; Rare:31 | ||||
chr2:5691295-5691428 | Rare:38 |