| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:156640575-156640855 | Common:3; Rare:117 | ||||
| chr8:1755620-1755865 | Common:5; Rare:72 | ||||
| chr8:6406540-6406668 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708189-6708424 | Common:3; Rare:102 | ||||
| chr8:17246791-17247077 | Common:2; Rare:119 | ||||
| chr8:22245024-22245141 | Rare:63 | ||||
| chr8:22579018-22579136 | Rare:29 | ||||
| chr8:22589252-22589362 | Rare:47 | ||||
| chr8:23287795-23288155 | Common:2; Rare:102 | ||||
| chr8:23457607-23457771 | Common:3; Rare:66 | ||||
| chr8:26382964-26383123 | Common:2; Rare:72 | ||||
| chr8:30095453-30095510 | Rare:23 | ||||
| chr8:30156239-30156384 | Common:1; Rare:40 | ||||
| chr8:31033603-31033872 | Common:3; Rare:65; Clinvar:5; Clinvar (benign):3 | ||||
| chr8:33485001-33485204 | Common:3; Rare:73 |