| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42152763-42153104 | Common:3; Rare:90 | ||||
| chr8:42338385-42338520 | Common:1; Rare:59 | ||||
| chr8:42391529-42391925 | Common:4; Rare:120 | ||||
| chr8:42541067-42541178 | Rare:27 | ||||
| chr8:42541494-42541750 | Common:2; Rare:79 | ||||
| chr8:42541893-42541950 | Rare:15; Clinvar:1 | ||||
| chr8:42842789-42843026 | Common:2; Rare:77; Clinvar (benign):1 | ||||
| chr8:42843028-42843099 | Rare:17; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr8:42843239-42843523 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:42896573-42897028 | Common:1; Rare:183 | ||||
| chr8:42897273-42897447 | Common:1; Rare:49 | ||||
| chr8:43056076-43056497 | Common:2; Rare:143 | ||||
| chr8:43093369-43093555 | Common:3; Rare:37; Clinvar (benign):1 | ||||
| chr8:47260781-47260991 | Common:3; Rare:93 | ||||
| chr8:47960049-47960267 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):3 |