| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4538409-4538963 | Common:18; Rare:750 | ||||
| chr12:4561968-4562368 | Common:7; Rare:228 | ||||
| chr12:4604501-4605131 | Common:13; Rare:343 | ||||
| chr12:4648835-4649541 | Common:12; Rare:506; Clinvar (benign):11 | ||||
| chr12:6199888-6200550 | Common:11; Rare:412 | ||||
| chr12:6310428-6310828 | Common:6; Rare:142 | ||||
| chr12:6340756-6341590 | Common:9; Rare:278 | ||||
| chr12:6341573-6341973 | Common:2; Rare:97; Clinvar:2; Clinvar (benign):3 | ||||
| chr12:6341957-6342240 | Common:1; Rare:135; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6342290-6342690 | Common:3; Rare:63; Clinvar:1 | ||||
| chr12:6363160-6363587 | Common:7; Rare:344; Clinvar:3; Clinvar (benign):4 | ||||
| chr12:6363613-6364051 | Common:7; Rare:314 | ||||
| chr12:6383790-6384370 | Common:14; Rare:482 | ||||
| chr12:6384366-6384766 | Common:3; Rare:104 | ||||
| chr12:6384778-6385092 | Common:3; Rare:95 |