| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:47960112-47960252 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr8:47960683-47961000 | Common:2; Rare:121; Clinvar:10; Clinvar (benign):1 | ||||
| chr8:48008366-48008457 | Common:1; Rare:60 | ||||
| chr8:51899001-51899331 | Common:6; Rare:147 | ||||
| chr8:52714371-52714563 | Common:1; Rare:81 | ||||
| chr8:53843212-53843365 | Rare:39 | ||||
| chr8:54022240-54022510 | Common:1; Rare:86 | ||||
| chr8:55773371-55773523 | Common:3; Rare:59 | ||||
| chr8:56074108-56074276 | Common:5; Rare:81 | ||||
| chr8:56074385-56074673 | Common:4; Rare:123 | ||||
| chr8:58659334-58659353 | Rare:7 | ||||
| chr8:59119111-59119256 | Rare:39 | ||||
| chr8:60516841-60517198 | Common:1; Rare:116 | ||||
| chr8:61714398-61714916 | Common:3; Rare:163 | ||||
| chr8:63038750-63038978 | Common:3; Rare:82 |