| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:175168121-175168444 | Common:1; Rare:88 | ||||
| chr2:175181629-175181779 | Common:4; Rare:64 | ||||
| chr2:176002232-176002398 | Common:2; Rare:69 | ||||
| chr2:176093263-176093299 | Common:1; Rare:11; Clinvar (benign):1 | ||||
| chr2:176129623-176129745 | Rare:63 | ||||
| chr2:176269386-176269537 | Common:1; Rare:59 | ||||
| chr2:177212402-177212813 | Common:5; Rare:168 | ||||
| chr2:177213162-177213261 | Rare:41 | ||||
| chr2:177263427-177263660 | Common:1; Rare:54 | ||||
| chr2:177264642-177264860 | Common:2; Rare:71 | ||||
| chr2:177392657-177393046 | Common:3; Rare:140; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552761-177552855 | Common:1; Rare:32 | ||||
| chr2:177618708-177619018 | Common:7; Rare:83 | ||||
| chr2:178450693-178450885 | Common:1; Rare:65 | ||||
| chr2:178451090-178451346 | Common:6; Rare:76; Clinvar:4; Clinvar (benign):3 |