| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:20217330-20217610 | Common:2; Rare:111 | ||||
| chr7:20330452-20331360 | Common:7; Rare:392 | ||||
| chr7:20331261-20331499 | Common:1; Rare:59 | ||||
| chr7:20331670-20331920 | Common:4; Rare:149 | ||||
| chr7:21427222-21427553 | Common:10; Rare:221 | ||||
| chr7:21427760-21428244 | Common:9; Rare:323 | ||||
| chr7:21945268-21945690 | Common:5; Rare:181 | ||||
| chr7:21945820-21946211 | Common:3; Rare:128 | ||||
| chr7:22726365-22726765 | Common:5; Rare:73 | ||||
| chr7:22726982-22727252 | Common:3; Rare:66 | ||||
| chr7:22822701-22822988 | Common:7; Rare:185 | ||||
| chr7:23105636-23105860 | Common:8; Rare:234; Clinvar:4; Clinvar (benign):6 | ||||
| chr7:23181816-23182175 | Common:4; Rare:266 | ||||
| chr7:23299144-23299409 | Common:6; Rare:243 | ||||
| chr7:23467750-23468210 | Common:5; Rare:169 |