| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98593484-98593790 | Common:2; Rare:101; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644697-98644843 | Common:3; Rare:49 | ||||
| chr12:98644982-98645313 | Common:2; Rare:98 | ||||
| chr12:100199982-100200279 | Common:1; Rare:68 | ||||
| chr12:100200563-100200854 | Common:3; Rare:87 | ||||
| chr12:100267047-100267434 | Common:2; Rare:159 | ||||
| chr12:100573554-100573740 | Rare:65 | ||||
| chr12:101407672-101408076 | Common:3; Rare:99 | ||||
| chr12:101697534-101697685 | Common:2; Rare:46 | ||||
| chr12:101790084-101790127 | Rare:7 | ||||
| chr12:101830557-101830777 | Common:4; Rare:81; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr12:101877515-101877729 | Common:3; Rare:58 | ||||
| chr12:102120061-102120254 | Rare:76 | ||||
| chr12:103841024-103841468 | Common:6; Rare:136 | ||||
| chr12:103929990-103930563 | Common:9; Rare:187 |