| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:96261544-96261967 | Common:6; Rare:145 | ||||
| chr8:97644467-97644862 | Common:2; Rare:130 | ||||
| chr8:97775697-97776090 | Common:7; Rare:191; Clinvar (benign):1 | ||||
| chr8:98045336-98045666 | Common:3; Rare:98 | ||||
| chr8:98117083-98117379 | Common:4; Rare:97 | ||||
| chr8:98944248-98944452 | Common:1; Rare:63 | ||||
| chr8:99013000-99013339 | Rare:67 | ||||
| chr8:100150522-100150716 | Common:1; Rare:65 | ||||
| chr8:100309856-100310296 | Common:1; Rare:152 | ||||
| chr8:100706649-100706997 | Common:10; Rare:92 | ||||
| chr8:100950399-100950722 | Common:11; Rare:128 | ||||
| chr8:100951252-100951421 | Rare:59 | ||||
| chr8:100952419-100952567 | Rare:44 | ||||
| chr8:100953319-100953440 | Common:1; Rare:26 | ||||
| chr8:101204699-101204842 | Common:1; Rare:28 |