| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:69096380-69096620 | Common:2; Rare:54 | ||||
| chr4:69495753-69496154 | Common:3; Rare:90 | ||||
| chr4:69760508-69760776 | Rare:48 | ||||
| chr4:70688201-70688586 | Common:2; Rare:96 | ||||
| chr4:70839236-70839419 | Common:2; Rare:80 | ||||
| chr4:70902124-70902459 | Common:6; Rare:114 | ||||
| chr4:70993327-70993831 | Common:6; Rare:148 | ||||
| chr4:71187077-71187312 | Common:1; Rare:73 | ||||
| chr4:71783935-71784128 | Common:1; Rare:57 | ||||
| chr4:71784130-71784365 | Rare:44 | ||||
| chr4:71803924-71804070 | Common:1; Rare:37 | ||||
| chr4:73104185-73104383 | Common:1; Rare:36 | ||||
| chr4:73258532-73258910 | Common:1; Rare:115 | ||||
| chr4:73259092-73259280 | Common:1; Rare:53 | ||||
| chr4:73409343-73409568 | Common:1; Rare:58; Clinvar:3; Clinvar (benign):1 |