| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:11802422-11802803 | Common:6; Rare:212 | ||||
| chr8:13566760-13566908 | Common:6; Rare:56 | ||||
| chr8:17246789-17247012 | Common:2; Rare:97 | ||||
| chr8:17413338-17413504 | Common:1; Rare:79 | ||||
| chr8:17922669-17923006 | Common:4; Rare:130 | ||||
| chr8:18084810-18084859 | Common:1; Rare:21; Clinvar (benign):1 | ||||
| chr8:18084921-18085027 | Rare:25 | ||||
| chr8:19013637-19013983 | Common:5; Rare:101 | ||||
| chr8:19817204-19817515 | Common:6; Rare:109 | ||||
| chr8:21919530-21919763 | Common:2; Rare:99 | ||||
| chr8:22245023-22245441 | Common:2; Rare:148 | ||||
| chr8:22367097-22367286 | Common:4; Rare:65 | ||||
| chr8:22669063-22669221 | Common:2; Rare:57 | ||||
| chr8:23069011-23069184 | Rare:67 | ||||
| chr8:23164022-23164252 | Rare:46 |