| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21437578-21437725 | Common:5; Rare:60 | ||||
| chr12:21501505-21501906 | Common:6; Rare:111 | ||||
| chr12:21657739-21657976 | Common:4; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21941411-21941428 | Rare:4 | ||||
| chr12:22046455-22046561 | Rare:30 | ||||
| chr12:22376831-22377026 | Common:4; Rare:67 | ||||
| chr12:22544142-22544321 | Common:1; Rare:91 | ||||
| chr12:22544466-22544735 | Common:2; Rare:60 | ||||
| chr12:22624977-22625520 | Common:2; Rare:204 | ||||
| chr12:22625555-22625846 | Common:3; Rare:81 | ||||
| chr12:23584561-23584708 | Common:1; Rare:43 | ||||
| chr12:23738493-23738673 | Common:3; Rare:31 | ||||
| chr12:24830311-24830381 | Rare:10 | ||||
| chr12:24948994-24949215 | Common:1; Rare:52 | ||||
| chr12:24949326-24949455 | Rare:25 |