| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99498736-99498759 | Rare:6 | ||||
| chr13:102117120-102117439 | Common:1; Rare:59 | ||||
| chr13:102394502-102394646 | Common:1; Rare:53 | ||||
| chr13:109265148-109265504 | Common:5; Rare:79 | ||||
| chr13:109268949-109269210 | Common:9; Rare:44 | ||||
| chr13:109269518-109269709 | Common:2; Rare:42 | ||||
| chr13:109272034-109272220 | Common:5; Rare:45 | ||||
| chr13:110308524-110308610 | Common:1; Rare:15 | ||||
| chr13:110616408-110616436 | Common:1; Rare:11 | ||||
| chr14:20456825-20457223 | Common:2; Rare:159; Clinvar:1 | ||||
| chr14:21017542-21017946 | Common:1; Rare:132 | ||||
| chr14:22770572-22770909 | Common:2; Rare:79 | ||||
| chr14:24248330-24248412 | Rare:7 | ||||
| chr14:24258275-24258692 | Rare:112; Clinvar:4; Clinvar (pathogenic):7 | ||||
| chr14:24259073-24259409 | Common:1; Rare:79; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):5 |