| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112125314-112125631 | Rare:76 | ||||
| chr12:112382367-112382592 | Common:1; Rare:77 | ||||
| chr12:112408757-112408836 | Rare:15 | ||||
| chr12:112409135-112409391 | Common:1; Rare:67 | ||||
| chr12:112409471-112409721 | Common:1; Rare:81 | ||||
| chr12:112418710-112419025 | Common:1; Rare:98; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:112419135-112419423 | Common:2; Rare:70; Clinvar (benign):2 | ||||
| chr12:112906802-112907251 | Common:1; Rare:120 | ||||
| chr12:112907504-112907729 | Rare:34 | ||||
| chr12:112937927-112938052 | Common:1; Rare:15 | ||||
| chr12:112938385-112938873 | Common:6; Rare:121 | ||||
| chr12:112978079-112978400 | Common:1; Rare:64 | ||||
| chr12:112978411-112978836 | Common:1; Rare:99 | ||||
| chr12:113089522-113089622 | Common:2; Rare:20 | ||||
| chr12:113184896-113185240 | Common:2; Rare:88 |