| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176269317-176269516 | Common:1; Rare:79 | ||||
| chr2:177212416-177212810 | Common:4; Rare:160 | ||||
| chr2:177392651-177393070 | Common:3; Rare:144; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552761-177552838 | Common:1; Rare:29 | ||||
| chr2:177618708-177619018 | Common:7; Rare:83 | ||||
| chr2:178194393-178194662 | Common:2; Rare:71 | ||||
| chr2:178451026-178451310 | Common:8; Rare:85; Clinvar:5; Clinvar (benign):5 | ||||
| chr2:178478504-178478659 | Common:1; Rare:47 | ||||
| chr2:180980245-180980545 | Common:1; Rare:94 | ||||
| chr2:181891675-181892049 | Common:4; Rare:153 | ||||
| chr2:182716359-182716406 | Rare:7 | ||||
| chr2:183124252-183124460 | Common:4; Rare:71 | ||||
| chr2:186485983-186486376 | Common:3; Rare:113 | ||||
| chr2:186590077-186590350 | Rare:82 | ||||
| chr2:187554345-187554486 | Rare:31 |