| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7108497-7108701 | Common:1; Rare:51 | ||||
| chr12:7130273-7130459 | Common:4; Rare:49 | ||||
| chr12:7189539-7189750 | Common:1; Rare:77; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:8032584-8032738 | Common:2; Rare:58 | ||||
| chr12:8697809-8698072 | Common:1; Rare:102 | ||||
| chr12:8780259-8780476 | Common:2; Rare:40 | ||||
| chr12:8949538-8950104 | Common:4; Rare:133 | ||||
| chr12:10613456-10613682 | Common:1; Rare:87 | ||||
| chr12:11170900-11171225 | Common:4; Rare:83 | ||||
| chr12:11171241-11171390 | Common:6; Rare:39 | ||||
| chr12:11171559-11171724 | Common:2; Rare:56 | ||||
| chr12:12356970-12357196 | Common:4; Rare:117 | ||||
| chr12:12506082-12506207 | Rare:20 | ||||
| chr12:12611654-12611991 | Common:2; Rare:101 | ||||
| chr12:12696146-12696270 | Rare:35 |