| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76348403-76348474 | Common:1; Rare:23; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76559696-76559884 | Rare:75 | ||||
| chr12:76764069-76764269 | Common:1; Rare:85 | ||||
| chr12:76879012-76879132 | Rare:33 | ||||
| chr12:77065509-77065766 | Common:1; Rare:86 | ||||
| chr12:79690513-79690687 | Common:1; Rare:49 | ||||
| chr12:79690965-79691221 | Common:1; Rare:85 | ||||
| chr12:79934787-79935355 | Common:1; Rare:205 | ||||
| chr12:82358322-82358549 | Rare:106 | ||||
| chr12:82358727-82358905 | Common:3; Rare:90 | ||||
| chr12:88142043-88142390 | Rare:95; Clinvar:3 | ||||
| chr12:88580466-88580552 | Common:1; Rare:27 | ||||
| chr12:89352474-89352711 | Rare:73 | ||||
| chr12:92145836-92146144 | Common:2; Rare:91 | ||||
| chr12:92929281-92929503 | Rare:65 |