| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:48420456-48420758 | Common:2; Rare:51 | ||||
| chr8:56072791-56073063 | Common:1; Rare:72 | ||||
| chr8:58566182-58566477 | Common:1; Rare:34 | ||||
| chr8:58583429-58583533 | Common:1; Rare:30 | ||||
| chr8:60599912-60599981 | Rare:10 | ||||
| chr8:61644598-61644655 | Common:1; Rare:21 | ||||
| chr8:66922375-66922669 | Rare:82 | ||||
| chr8:66922692-66922728 | Rare:5 | ||||
| chr8:66925439-66925602 | Rare:56 | ||||
| chr8:67093340-67093645 | Rare:60; Clinvar (pathogenic):1 | ||||
| chr8:68772930-68773033 | Common:1; Rare:23 | ||||
| chr8:68816949-68816993 | Rare:12 | ||||
| chr8:68819903-68820264 | Common:1; Rare:53 | ||||
| chr8:68820646-68820956 | Common:3; Rare:56 | ||||
| chr8:68821754-68821994 | Common:3; Rare:52 |