| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:30156243-30156439 | Rare:59 | ||||
| chr8:30384149-30384575 | Common:1; Rare:114 | ||||
| chr8:30658014-30658413 | Common:5; Rare:114 | ||||
| chr8:30744093-30744424 | Common:4; Rare:111 | ||||
| chr8:33485052-33485219 | Common:2; Rare:59 | ||||
| chr8:37762509-37762700 | Common:2; Rare:78 | ||||
| chr8:37849823-37850002 | Common:1; Rare:66 | ||||
| chr8:37966574-37966720 | Rare:40 | ||||
| chr8:38030269-38030595 | Common:3; Rare:94 | ||||
| chr8:38105340-38105563 | Common:2; Rare:67 | ||||
| chr8:38105719-38105966 | Common:1; Rare:76 | ||||
| chr8:38176430-38176541 | Common:1; Rare:40 | ||||
| chr8:38176676-38176875 | Common:2; Rare:56 | ||||
| chr8:38269121-38269431 | Rare:104 | ||||
| chr8:38467999-38468168 | Rare:45; Clinvar (benign):2 |