| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:175181355-175181781 | Common:7; Rare:151 | ||||
| chr2:176002170-176002406 | Common:4; Rare:99 | ||||
| chr2:176269339-176269452 | Common:1; Rare:37 | ||||
| chr2:177212492-177212820 | Common:3; Rare:133 | ||||
| chr2:177213145-177213290 | Rare:69 | ||||
| chr2:177216582-177217151 | Common:2; Rare:172 | ||||
| chr2:177263401-177263709 | Common:1; Rare:76 | ||||
| chr2:177264057-177264326 | Rare:74 | ||||
| chr2:177264547-177265015 | Common:2; Rare:127 | ||||
| chr2:177392659-177393082 | Common:3; Rare:145; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177618721-177618757 | Common:1; Rare:12 | ||||
| chr2:177618922-177619037 | Common:1; Rare:29 | ||||
| chr2:178451029-178451451 | Common:8; Rare:125; Clinvar:5; Clinvar (benign):4 | ||||
| chr2:178478535-178478628 | Rare:29 | ||||
| chr2:178480754-178480888 | Common:1; Rare:41 |