| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56152435-56152620 | Rare:55 | ||||
| chr12:64759380-64759585 | Common:1; Rare:63; Clinvar:3 | ||||
| chr12:71663823-71664118 | Common:1; Rare:75 | ||||
| chr12:75390899-75391089 | Common:1; Rare:52 | ||||
| chr12:82358385-82358549 | Rare:64 | ||||
| chr12:91182612-91182672 | Rare:15 | ||||
| chr12:106955738-106955923 | Rare:65 | ||||
| chr12:109477293-109477382 | Common:2; Rare:37 | ||||
| chr12:109573484-109573814 | Common:3; Rare:94; Clinvar:3; Clinvar (benign):5 | ||||
| chr12:112013153-112013456 | Common:1; Rare:102 | ||||
| chr12:113185463-113185584 | Common:4; Rare:50 | ||||
| chr12:120446359-120446459 | Common:1; Rare:45 | ||||
| chr12:123233134-123233481 | Common:2; Rare:106; Clinvar:1 | ||||
| chr12:123633597-123633840 | Common:1; Rare:118; Clinvar:8; Clinvar (benign):1 | ||||
| chr13:41060935-41061253 | Common:8; Rare:127 |