| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:55107226-55107394 | Rare:28 | ||||
| chr7:55114761-55114868 | Common:1; Rare:13 | ||||
| chr7:55133826-55133878 | Common:1; Rare:6 | ||||
| chr7:55135555-55135712 | Common:2; Rare:24 | ||||
| chr7:55156532-55156830 | Rare:64; Clinvar:1 | ||||
| chr7:55172827-55173121 | Common:1; Rare:101; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:55184336-55184601 | Common:4; Rare:34 | ||||
| chr7:55191697-55191749 | Rare:17; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:55194018-55194212 | Common:2; Rare:44 | ||||
| chr7:55200925-55201278 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:55453600-55453696 | Common:1; Rare:17 | ||||
| chr7:55454143-55454177 | Rare:3 | ||||
| chr7:55459726-55459769 | Rare:10 | ||||
| chr7:55459830-55460217 | Common:12; Rare:53 | ||||
| chr7:55463315-55463436 | Common:2; Rare:22 |