| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57229451-57229851 | Common:11; Rare:492 | ||||
| chr12:57229950-57230471 | Rare:507 | ||||
| chr12:57237264-57237664 | Rare:110 | ||||
| chr12:57239901-57240814 | Common:13; Rare:711 | ||||
| chr12:57430081-57430780 | Common:9; Rare:414 | ||||
| chr12:57430745-57431410 | Common:22; Rare:951 | ||||
| chr12:57431434-57431834 | Common:1; Rare:82 | ||||
| chr12:57452013-57453028 | Common:7; Rare:266 | ||||
| chr12:57454443-57454843 | Common:1; Rare:330 | ||||
| chr12:57454925-57455528 | Rare:408 | ||||
| chr12:57455737-57456952 | Common:4; Rare:814 | ||||
| chr12:57477720-57478290 | Common:4; Rare:286 | ||||
| chr12:57478280-57478880 | Common:3; Rare:328; Clinvar:2 | ||||
| chr12:57487730-57488811 | Common:10; Rare:683; Clinvar:16; Clinvar (benign):9 | ||||
| chr12:57488723-57489123 | Common:12; Rare:253; Clinvar (benign):6 |