| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112125429-112125574 | Rare:41 | ||||
| chr12:113185447-113185775 | Common:8; Rare:114 | ||||
| chr12:113966202-113966530 | Common:9; Rare:109 | ||||
| chr12:118135942-118136195 | Common:2; Rare:78 | ||||
| chr12:119877269-119877557 | Common:2; Rare:64 | ||||
| chr12:120116740-120116895 | Rare:45 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120437881-120438196 | Common:2; Rare:120; Clinvar (benign):2 | ||||
| chr12:120446344-120446483 | Common:1; Rare:63 | ||||
| chr12:120469616-120469895 | Common:3; Rare:99 | ||||
| chr12:120495859-120496272 | Common:7; Rare:141 | ||||
| chr12:120581358-120581588 | Common:1; Rare:81 | ||||
| chr12:121352385-121352655 | Common:2; Rare:64 | ||||
| chr12:121399850-121400155 | Common:5; Rare:114 | ||||
| chr12:122422544-122422828 | Common:4; Rare:92 |