| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109900255-109900356 | Rare:35 | ||||
| chr12:110281024-110281193 | Rare:66 | ||||
| chr12:110468721-110468909 | Rare:52 | ||||
| chr12:110501304-110501622 | Common:1; Rare:80 | ||||
| chr12:110502047-110502195 | Common:1; Rare:54 | ||||
| chr12:110613953-110614212 | Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:111685743-111686110 | Rare:134 | ||||
| chr12:111766816-111767049 | Rare:73 | ||||
| chr12:111841900-111842040 | Common:1; Rare:40 | ||||
| chr12:112013125-112013467 | Common:1; Rare:121 | ||||
| chr12:113185429-113185794 | Common:9; Rare:132 | ||||
| chr12:113221039-113221280 | Common:1; Rare:63 | ||||
| chr12:114405788-114405883 | Common:1; Rare:14 | ||||
| chr12:114407995-114408208 | Common:1; Rare:37; Clinvar (benign):2 | ||||
| chr12:118135938-118136260 | Common:2; Rare:96 |