| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:117099369-117099539 | Common:1; Rare:55 | ||||
| chr12:117190218-117190328 | Rare:33 | ||||
| chr12:117968981-117969014 | Rare:12 | ||||
| chr12:118016408-118016828 | Common:4; Rare:78 | ||||
| chr12:118061042-118061473 | Common:5; Rare:97 | ||||
| chr12:118103839-118104121 | Common:1; Rare:72 | ||||
| chr12:118104334-118104656 | Common:1; Rare:45 | ||||
| chr12:118135935-118136305 | Common:2; Rare:115 | ||||
| chr12:118372799-118373220 | Common:2; Rare:120 | ||||
| chr12:118376488-118376806 | Common:1; Rare:102 | ||||
| chr12:119178615-119178994 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:119667934-119668040 | Rare:26 | ||||
| chr12:119877252-119877577 | Common:3; Rare:73 | ||||
| chr12:120116703-120116907 | Common:1; Rare:60 | ||||
| chr12:120194683-120194760 | Rare:29 |