| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:13479396-13479522 | Rare:25 | ||||
| chr3:13479956-13480413 | Common:16; Rare:521 | ||||
| chr3:13548930-13549210 | Common:1; Rare:93 | ||||
| chr3:14123924-14124589 | Common:12; Rare:410 | ||||
| chr3:14124669-14125152 | Common:24; Rare:757; Clinvar:24; Clinvar (benign):6 | ||||
| chr3:14177508-14177908 | Common:3; Rare:82 | ||||
| chr3:14178160-14178494 | Rare:165; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:14178510-14178980 | Common:17; Rare:1285; Clinvar:29; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr3:14401901-14402798 | Common:14; Rare:558 | ||||
| chr3:14402840-14403042 | Rare:68 | ||||
| chr3:14402967-14403490 | Common:3; Rare:157 | ||||
| chr3:14432240-14432700 | Common:4; Rare:149 | ||||
| chr3:14651316-14652170 | Common:7; Rare:949 | ||||
| chr3:14946730-14947650 | Common:30; Rare:1282 | ||||
| chr3:14947628-14948028 | Common:7; Rare:253 |