| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178608042-178608233 | Common:2; Rare:45; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:178645931-178646187 | Common:3; Rare:57; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:188975928-188975976 | Rare:12 | ||||
| chr2:188984719-188985501 | Common:6; Rare:181; Clinvar:13; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr2:188985576-188985792 | Rare:46; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:188988059-188988478 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
| chr2:188988515-188988648 | Rare:40; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):10 | ||||
| chr2:188989274-188989449 | Rare:38; Clinvar:2; Clinvar (pathogenic):5 | ||||
| chr2:188990020-188990419 | Rare:113; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr2:188993084-188993574 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr2:188994028-188994345 | Common:1; Rare:86; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
| chr2:188994479-188994649 | Rare:48; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr2:188994658-188995004 | Common:1; Rare:69; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:188995012-188995577 | Common:3; Rare:113; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr2:188995579-188995795 | Rare:57; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 |