| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:175167660-175167864 | Rare:67 | ||||
| chr2:175181659-175181776 | Common:3; Rare:50 | ||||
| chr2:176002254-176002407 | Common:2; Rare:61 | ||||
| chr2:176269307-176269500 | Common:1; Rare:77 | ||||
| chr2:177212382-177212802 | Common:5; Rare:171 | ||||
| chr2:177392643-177392823 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:177552761-177552841 | Common:1; Rare:29 | ||||
| chr2:177618708-177618753 | Common:1; Rare:18 | ||||
| chr2:178450718-178450897 | Rare:64 | ||||
| chr2:178451083-178451194 | Common:2; Rare:42; Clinvar:3 | ||||
| chr2:178478512-178478711 | Common:1; Rare:66 | ||||
| chr2:180007085-180007122 | Rare:8 | ||||
| chr2:181457244-181457383 | Rare:48 | ||||
| chr2:182715935-182716406 | Common:3; Rare:154 | ||||
| chr2:182866533-182866760 | Common:1; Rare:52 |