| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17810607-17811035 | Common:3; Rare:129 | ||||
| chr4:20252758-20252928 | Common:1; Rare:43 | ||||
| chr4:20254137-20254285 | Common:1; Rare:31 | ||||
| chr4:24584322-24584373 | Rare:18 | ||||
| chr4:24795342-24795625 | Common:1; Rare:66 | ||||
| chr4:25160376-25160732 | Common:3; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25234074 | Rare:98 | ||||
| chr4:25914051-25914321 | Common:2; Rare:115 | ||||
| chr4:26320597-26320852 | Common:1; Rare:104 | ||||
| chr4:26320870-26321043 | Rare:59; Clinvar (benign):1 | ||||
| chr4:30719883-30720432 | Common:4; Rare:116 | ||||
| chr4:30720538-30720638 | Rare:18 | ||||
| chr4:30720677-30720856 | Rare:36 | ||||
| chr4:30721164-30721443 | Common:3; Rare:70 | ||||
| chr4:30721978-30722173 | Common:1; Rare:63 |