| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121530568-121530880 | Common:7; Rare:125 | ||||
| chr2:127294137-127294235 | Common:2; Rare:31; Clinvar (benign):2 | ||||
| chr2:128091031-128091333 | Common:8; Rare:101 | ||||
| chr2:130181576-130181705 | Common:1; Rare:41 | ||||
| chr2:134918624-134918852 | Common:1; Rare:92 | ||||
| chr2:135531195-135531508 | Common:1; Rare:57 | ||||
| chr2:148020703-148021011 | Common:1; Rare:63 | ||||
| chr2:151828455-151828793 | Common:2; Rare:96 | ||||
| chr2:152717829-152717942 | Rare:47 | ||||
| chr2:152717991-152718078 | Rare:26 | ||||
| chr2:156436268-156436410 | Common:3; Rare:46 | ||||
| chr2:159712429-159712575 | Common:2; Rare:56 | ||||
| chr2:160493488-160493626 | Rare:39 | ||||
| chr2:161308380-161308543 | Common:2; Rare:39 | ||||
| chr2:165794142-165794331 | Common:2; Rare:56; Clinvar:6; Clinvar (benign):1 |