| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:41797561-41797716 | Common:2; Rare:46; Clinvar (pathogenic):2 | ||||
| chr8:42051976-42052263 | Common:1; Rare:84 | ||||
| chr8:42338377-42338509 | Common:1; Rare:54 | ||||
| chr8:42391521-42391928 | Common:4; Rare:121 | ||||
| chr8:42540939-42541179 | Rare:63 | ||||
| chr8:42541543-42541744 | Rare:69 | ||||
| chr8:42541895-42541931 | Rare:8 | ||||
| chr8:42843041-42843117 | Rare:23; Clinvar:3 | ||||
| chr8:42843227-42843469 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:42896596-42897043 | Common:1; Rare:180 | ||||
| chr8:42897288-42897472 | Common:1; Rare:53 | ||||
| chr8:43056105-43056466 | Common:1; Rare:127 | ||||
| chr8:43093440-43093550 | Common:2; Rare:23 | ||||
| chr8:47260781-47260981 | Common:3; Rare:87 | ||||
| chr8:47960106-47960230 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):2 |