| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6233214-6233484 | Common:1; Rare:60 | ||||
| chr12:6583259-6583505 | Rare:45 | ||||
| chr12:6770174-6770548 | Rare:102 | ||||
| chr12:6974127-6974399 | Rare:74 | ||||
| chr12:7089286-7089734 | Common:3; Rare:145 | ||||
| chr12:8242933-8243244 | Common:8; Rare:88 | ||||
| chr12:9065054-9065189 | Rare:14 | ||||
| chr12:9070531-9070838 | Common:3; Rare:54 | ||||
| chr12:9089206-9089285 | Rare:13 | ||||
| chr12:9109323-9109613 | Rare:60 | ||||
| chr12:9109865-9109867 | |||||
| chr12:9240318-9240400 | Common:1; Rare:17 | ||||
| chr12:9448187-9448276 | Rare:48 | ||||
| chr12:9647892-9648351 | Common:5; Rare:143 | ||||
| chr12:12718552-12718817 | Common:1; Rare:78; Clinvar (benign):1 |