| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109116106-109116702 | Common:5; Rare:110 | ||||
| chr12:109154557-109154734 | Common:1; Rare:49 | ||||
| chr12:109175928-109176261 | Rare:104 | ||||
| chr12:109477260-109477667 | Common:3; Rare:109 | ||||
| chr12:109573472-109573832 | Common:3; Rare:105; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:109880371-109880676 | Common:1; Rare:93 | ||||
| chr12:110280427-110280659 | Rare:56 | ||||
| chr12:110281024-110281264 | Rare:87 | ||||
| chr12:110281659-110281949 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr12:110468764-110468923 | Rare:49 | ||||
| chr12:110502051-110502158 | Common:1; Rare:46 | ||||
| chr12:111685718-111686098 | Rare:137 | ||||
| chr12:111766823-111767019 | Rare:64 | ||||
| chr12:111841894-111842243 | Common:3; Rare:96 | ||||
| chr12:112013111-112013460 | Common:1; Rare:123 |