| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:175005163-175005331 | Rare:57; Clinvar:2 | ||||
| chr2:175168058-175168593 | Common:2; Rare:146 | ||||
| chr2:175181620-175181779 | Common:4; Rare:64 | ||||
| chr2:176002221-176002414 | Common:3; Rare:85 | ||||
| chr2:176129573-176129721 | Rare:87 | ||||
| chr2:176188501-176188668 | Common:1; Rare:64 | ||||
| chr2:177212416-177212821 | Common:4; Rare:164 | ||||
| chr2:177216188-177216590 | Rare:133 | ||||
| chr2:177216803-177216940 | Rare:44 | ||||
| chr2:177263402-177263725 | Common:2; Rare:78 | ||||
| chr2:177264531-177264854 | Common:2; Rare:93 | ||||
| chr2:177264897-177264965 | Rare:21 | ||||
| chr2:177264972-177265291 | Common:2; Rare:70 | ||||
| chr2:177392634-177393101 | Common:3; Rare:154; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552761-177552826 | Rare:27 |