| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49568579-49568663 | Common:1; Rare:15 | ||||
| chr12:49623188-49623581 | Common:3; Rare:109 | ||||
| chr12:49707283-49707493 | Common:2; Rare:59 | ||||
| chr12:49741238-49741676 | Rare:121 | ||||
| chr12:49742180-49742212 | Rare:15 | ||||
| chr12:49750445-49750619 | Rare:28 | ||||
| chr12:49828366-49828693 | Common:1; Rare:103 | ||||
| chr12:49842385-49842678 | Rare:50 | ||||
| chr12:49842831-49842935 | Rare:27 | ||||
| chr12:49843001-49843295 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr12:50025372-50025841 | Common:2; Rare:121 | ||||
| chr12:50084985-50085414 | Common:1; Rare:110 | ||||
| chr12:50085450-50085578 | Rare:27 | ||||
| chr12:50111648-50111870 | Rare:50 | ||||
| chr12:50112026-50112346 | Common:2; Rare:71; Clinvar (benign):1 |