| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:20330898-20331062 | Common:2; Rare:43 | ||||
| chr7:22727071-22727348 | Common:1; Rare:60 | ||||
| chr7:22727656-22727751 | Common:1; Rare:35 | ||||
| chr7:22728535-22728805 | Common:2; Rare:71 | ||||
| chr7:22822671-22822921 | Common:2; Rare:97 | ||||
| chr7:23013920-23014161 | Common:1; Rare:108; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:23105671-23105890 | Common:3; Rare:112; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:23106034-23106123 | Rare:22 | ||||
| chr7:23181757-23182203 | Common:3; Rare:175 | ||||
| chr7:23299423-23299588 | Rare:71 | ||||
| chr7:23467885-23468146 | Common:3; Rare:68 | ||||
| chr7:23469742-23470120 | Common:1; Rare:116 | ||||
| chr7:23470163-23470605 | Common:2; Rare:123 | ||||
| chr7:23531768-23532123 | Common:2; Rare:137 | ||||
| chr7:24980067-24980380 | Common:6; Rare:128 |