| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176848839-176848936 | Common:1; Rare:17 | ||||
| chr2:176849345-176849494 | Common:3; Rare:25 | ||||
| chr2:177008556-177008749 | Common:3; Rare:62 | ||||
| chr2:177476592-177476723 | Rare:22 | ||||
| chr2:177552168-177552428 | Common:1; Rare:93 | ||||
| chr2:177552462-177552511 | Common:1; Rare:20 | ||||
| chr2:178413873-178413994 | Rare:37 | ||||
| chr2:178523066-178523246 | Rare:59 | ||||
| chr2:178617191-178617373 | Common:1; Rare:45; Clinvar:7; Clinvar (benign):2 | ||||
| chr2:178633516-178633799 | Common:1; Rare:53; Clinvar:6; Clinvar (benign):8 | ||||
| chr2:178688695-178688908 | Common:1; Rare:48; Clinvar:3 | ||||
| chr2:179400501-179400709 | Rare:47 | ||||
| chr2:180691883-180692017 | Common:1; Rare:28 | ||||
| chr2:182609197-182609370 | Common:1; Rare:39 | ||||
| chr2:182866344-182866391 | Rare:14 |