| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:69189500-69189652 | Common:1; Rare:50 | ||||
| chr5:69217623-69217844 | Common:4; Rare:71 | ||||
| chr5:69332760-69332851 | Rare:25 | ||||
| chr5:69369473-69369885 | Common:1; Rare:164 | ||||
| chr5:69369961-69370052 | Common:1; Rare:23 | ||||
| chr5:69492659-69492811 | Rare:50; Clinvar (benign):1 | ||||
| chr5:69560002-69560293 | Common:3; Rare:75 | ||||
| chr5:71455529-71455697 | Rare:49 | ||||
| chr5:71587135-71587430 | Common:1; Rare:102; Clinvar (benign):2 | ||||
| chr5:72308329-72308636 | Common:3; Rare:86 | ||||
| chr5:72816524-72816704 | Common:3; Rare:66 | ||||
| chr5:72955860-72956080 | Common:1; Rare:99 | ||||
| chr5:73498282-73498652 | Common:3; Rare:118 | ||||
| chr5:73565606-73565826 | Common:5; Rare:96 | ||||
| chr5:74640543-74640966 | Common:3; Rare:133 |