| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110502058-110502336 | Common:1; Rare:102 | ||||
| chr12:110613991-110614269 | Rare:91; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:111685737-111686110 | Rare:135 | ||||
| chr12:111841847-111842026 | Common:2; Rare:55 | ||||
| chr12:112013110-112013478 | Common:1; Rare:134 | ||||
| chr12:112125347-112125578 | Rare:63 | ||||
| chr12:112409528-112409707 | Common:1; Rare:62 | ||||
| chr12:112906881-112907006 | Rare:26 | ||||
| chr12:113185435-113185777 | Common:8; Rare:124 | ||||
| chr12:113422318-113422408 | Common:1; Rare:21 | ||||
| chr12:113966315-113966540 | Common:9; Rare:78 | ||||
| chr12:117361624-117361664 | Rare:6 | ||||
| chr12:117968262-117968460 | Common:1; Rare:58 | ||||
| chr12:117969103-117969419 | Common:3; Rare:85 | ||||
| chr12:118016475-118016792 | Common:3; Rare:61 |