| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:94656003-94656601 | Common:4; Rare:205; Clinvar:12; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr7:94907442-94907769 | Common:3; Rare:119 | ||||
| chr7:95395980-95396260 | Common:4; Rare:140 | ||||
| chr7:95396294-95396680 | Common:4; Rare:251 | ||||
| chr7:95434890-95435162 | Common:2; Rare:228; Clinvar (benign):2 | ||||
| chr7:96321960-96322273 | Rare:251; Clinvar:8 | ||||
| chr7:96709707-96709925 | Common:1; Rare:125 | ||||
| chr7:97005436-97005612 | Common:2; Rare:93 | ||||
| chr7:97006377-97006639 | Common:1; Rare:82 | ||||
| chr7:97117414-97117774 | Common:3; Rare:281 | ||||
| chr7:97872356-97872581 | Common:2; Rare:136 | ||||
| chr7:98252125-98252426 | Common:4; Rare:138 | ||||
| chr7:98281170-98281805 | Common:11; Rare:302 | ||||
| chr7:98878388-98878621 | Rare:84 | ||||
| chr7:98878769-98878967 | Common:1; Rare:49 |