| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:11868003-11868316 | Rare:273 | ||||
| chr8:12753998-12754211 | Common:2; Rare:150 | ||||
| chr8:12755423-12755805 | Rare:312 | ||||
| chr8:13133051-13133829 | Common:27; Rare:308 | ||||
| chr8:13276245-13276834 | Common:5; Rare:299 | ||||
| chr8:17027125-17027293 | Common:4; Rare:162 | ||||
| chr8:17246295-17246695 | Common:6; Rare:225 | ||||
| chr8:17246776-17247085 | Common:4; Rare:248 | ||||
| chr8:17496783-17497207 | Common:10; Rare:271 | ||||
| chr8:17576930-17577240 | Common:4; Rare:84 | ||||
| chr8:17800791-17801450 | Common:20; Rare:320 | ||||
| chr8:17909620-17910280 | Common:10; Rare:215 | ||||
| chr8:17910340-17910606 | Common:5; Rare:121 | ||||
| chr8:17922494-17923071 | Common:12; Rare:425 | ||||
| chr8:18084070-18084610 | Common:11; Rare:300; Clinvar:9; Clinvar (benign):4 |