| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:10839797-10840094 | Common:2; Rare:102 | ||||
| chr8:11284719-11284861 | Common:2; Rare:59 | ||||
| chr8:11802450-11802767 | Common:6; Rare:166 | ||||
| chr8:17246583-17247042 | Common:5; Rare:195 | ||||
| chr8:18854190-18854338 | Common:1; Rare:35 | ||||
| chr8:19013643-19013961 | Common:4; Rare:92 | ||||
| chr8:22245024-22245444 | Common:2; Rare:150 | ||||
| chr8:22367196-22367327 | Common:5; Rare:59 | ||||
| chr8:22604526-22604820 | Common:1; Rare:111 | ||||
| chr8:22669082-22669232 | Common:2; Rare:52 | ||||
| chr8:23457601-23457791 | Common:3; Rare:68 | ||||
| chr8:23528609-23529057 | Rare:133 | ||||
| chr8:23706544-23706873 | Common:1; Rare:80; Clinvar (benign):1 | ||||
| chr8:26382928-26383118 | Common:1; Rare:88 | ||||
| chr8:26513874-26514025 | Rare:27 |