| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25914028-25914308 | Common:2; Rare:121 | ||||
| chr4:26320570-26321046 | Common:1; Rare:181; Clinvar (benign):1 | ||||
| chr4:26583663-26583913 | Common:1; Rare:43 | ||||
| chr4:26583918-26583965 | Rare:10 | ||||
| chr4:26583971-26584174 | Rare:49 | ||||
| chr4:26860607-26860812 | Common:2; Rare:69 | ||||
| chr4:30719942-30720099 | Common:1; Rare:29 | ||||
| chr4:30720176-30720422 | Common:2; Rare:60 | ||||
| chr4:30720613-30720905 | Rare:60 | ||||
| chr4:30721112-30721434 | Common:3; Rare:78 | ||||
| chr4:30721957-30722116 | Rare:46 | ||||
| chr4:30723019-30723193 | Common:1; Rare:47 | ||||
| chr4:38664190-38664330 | Common:1; Rare:45 | ||||
| chr4:38664802-38664999 | Rare:68 | ||||
| chr4:39182202-39182562 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):1 |