| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112005958-112006145 | Common:3; Rare:28 | ||||
| chr12:112013125-112013478 | Common:1; Rare:126 | ||||
| chr12:112013586-112013607 | Rare:10 | ||||
| chr12:112013889-112014157 | Rare:58 | ||||
| chr12:112108741-112108914 | Common:1; Rare:44 | ||||
| chr12:112409554-112409707 | Common:1; Rare:52 | ||||
| chr12:112906845-112906999 | Rare:27 | ||||
| chr12:113185391-113185810 | Common:10; Rare:159 | ||||
| chr12:113221019-113221319 | Common:2; Rare:86 | ||||
| chr12:113422179-113422443 | Common:3; Rare:60 | ||||
| chr12:113966288-113966523 | Common:8; Rare:81 | ||||
| chr12:114683638-114683913 | Common:1; Rare:54; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:114683922-114684353 | Common:4; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:114684493-114684674 | Rare:53 | ||||
| chr12:117099335-117099522 | Common:1; Rare:62 |