| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176104288-176104577 | Common:1; Rare:58 | ||||
| chr2:176108441-176108590 | Rare:37 | ||||
| chr2:176116603-176116906 | Common:2; Rare:79; Clinvar:1 | ||||
| chr2:176128999-176129402 | Rare:121 | ||||
| chr2:176129581-176129748 | Rare:91 | ||||
| chr2:176160617-176160786 | Common:2; Rare:23 | ||||
| chr2:176188490-176188668 | Common:1; Rare:69 | ||||
| chr2:176188911-176189169 | Common:2; Rare:104 | ||||
| chr2:176269353-176269505 | Common:1; Rare:64 | ||||
| chr2:177212416-177212863 | Common:4; Rare:174 | ||||
| chr2:177264563-177264826 | Common:2; Rare:76 | ||||
| chr2:177392651-177393090 | Common:3; Rare:148; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552761-177552838 | Common:1; Rare:29 | ||||
| chr2:178451027-178451381 | Common:9; Rare:102; Clinvar:5; Clinvar (benign):5 | ||||
| chr2:178478499-178478666 | Common:1; Rare:54 |