| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6341810-6342194 | Rare:77; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6375340-6375667 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6376168-6376440 | Common:3; Rare:59 | ||||
| chr12:6383957-6384281 | Common:2; Rare:77 | ||||
| chr12:6451780-6452120 | Common:4; Rare:62 | ||||
| chr12:6493088-6493394 | Common:7; Rare:90 | ||||
| chr12:6493778-6494126 | Common:2; Rare:104 | ||||
| chr12:6534416-6534571 | Common:5; Rare:70 | ||||
| chr12:6534626-6534860 | Common:3; Rare:96 | ||||
| chr12:6549108-6549278 | Common:1; Rare:29 | ||||
| chr12:6556039-6556212 | Common:3; Rare:64 | ||||
| chr12:6568241-6568393 | Rare:60 | ||||
| chr12:6688843-6689084 | Rare:74 | ||||
| chr12:6689121-6689175 | Rare:16 | ||||
| chr12:6689222-6689748 | Common:3; Rare:142 |