| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:100200707-100200834 | Rare:39 | ||||
| chr12:100267065-100267287 | Common:1; Rare:103 | ||||
| chr12:100573542-100573710 | Rare:56 | ||||
| chr12:101407719-101408040 | Common:3; Rare:78 | ||||
| chr12:102120069-102120235 | Rare:64 | ||||
| chr12:103930074-103930525 | Common:8; Rare:154 | ||||
| chr12:103965705-103965971 | Common:2; Rare:58 | ||||
| chr12:104064341-104064566 | Common:1; Rare:53 | ||||
| chr12:104138142-104138415 | Common:1; Rare:76 | ||||
| chr12:105236068-105236268 | Common:2; Rare:93 | ||||
| chr12:107320208-107320438 | Rare:49 | ||||
| chr12:108515005-108515289 | Common:1; Rare:83 | ||||
| chr12:109154535-109154686 | Common:1; Rare:40 | ||||
| chr12:109477287-109477653 | Common:3; Rare:90 | ||||
| chr12:109573468-109573845 | Common:3; Rare:112; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 |