| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12611626-12612128 | Common:3; Rare:141 | ||||
| chr12:12684470-12684627 | Common:1; Rare:22 | ||||
| chr12:12696141-12696296 | Rare:42 | ||||
| chr12:12696682-12696710 | Rare:11 | ||||
| chr12:12717242-12717476 | Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725642-12726042 | Common:4; Rare:99 | ||||
| chr12:12891306-12891567 | Common:1; Rare:52 | ||||
| chr12:13000196-13000486 | Common:2; Rare:92 | ||||
| chr12:13044325-13044400 | Rare:20 | ||||
| chr12:13196763-13196845 | Rare:16 | ||||
| chr12:14365482-14365771 | Common:1; Rare:90 | ||||
| chr12:14365801-14365880 | Rare:16 | ||||
| chr12:14365934-14366079 | Rare:40 | ||||
| chr12:14384933-14385321 | Common:1; Rare:74 | ||||
| chr12:14770030-14770104 | Rare:15 |