| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:15540143-15540441 | Common:5; Rare:110; Clinvar:11; Clinvar (benign):1 | ||||
| chr8:17246583-17247048 | Common:5; Rare:196 | ||||
| chr8:17922614-17923009 | Common:5; Rare:155 | ||||
| chr8:19013643-19013983 | Common:4; Rare:101 | ||||
| chr8:19084720-19084870 | Rare:35 | ||||
| chr8:21919499-21919773 | Common:2; Rare:112 | ||||
| chr8:22245024-22245164 | Rare:72 | ||||
| chr8:22669070-22669169 | Common:2; Rare:38 | ||||
| chr8:23068988-23069172 | Rare:75 | ||||
| chr8:23164010-23164118 | Rare:20 | ||||
| chr8:23404095-23404283 | Common:2; Rare:51 | ||||
| chr8:23457597-23457778 | Common:3; Rare:69 | ||||
| chr8:23854096-23854340 | Rare:49 | ||||
| chr8:25458413-25458732 | Common:3; Rare:95 | ||||
| chr8:26382935-26383201 | Common:3; Rare:121 |