| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:17246795-17247045 | Common:2; Rare:107 | ||||
| chr8:18084820-18084868 | Common:1; Rare:16; Clinvar (benign):1 | ||||
| chr8:22245026-22245171 | Common:1; Rare:73 | ||||
| chr8:23404116-23404294 | Common:2; Rare:43 | ||||
| chr8:23457639-23457778 | Common:2; Rare:50 | ||||
| chr8:26382971-26383123 | Common:2; Rare:70 | ||||
| chr8:26513874-26513989 | Rare:22 | ||||
| chr8:27772584-27772709 | Common:4; Rare:41 | ||||
| chr8:30095316-30095495 | Common:2; Rare:59 | ||||
| chr8:30156206-30156384 | Common:1; Rare:54 | ||||
| chr8:30744139-30744187 | Rare:24 | ||||
| chr8:33485087-33485204 | Common:1; Rare:41 | ||||
| chr8:37762478-37762662 | Common:2; Rare:63 | ||||
| chr8:38105356-38105539 | Common:2; Rare:50 | ||||
| chr8:38105766-38105929 | Rare:50 |