| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:95269389-95269616 | Common:3; Rare:60 | ||||
| chr8:96235510-96235652 | Common:1; Rare:74; Clinvar (benign):2 | ||||
| chr8:96261540-96261957 | Common:6; Rare:144 | ||||
| chr8:96493592-96494195 | Common:4; Rare:177 | ||||
| chr8:97644720-97644791 | Common:1; Rare:23 | ||||
| chr8:97775716-97776024 | Common:4; Rare:158; Clinvar (benign):1 | ||||
| chr8:98045337-98045679 | Common:4; Rare:102 | ||||
| chr8:98117032-98117361 | Common:4; Rare:118 | ||||
| chr8:99012991-99013343 | Rare:70 | ||||
| chr8:99893443-99893780 | Common:4; Rare:115 | ||||
| chr8:100150555-100150709 | Rare:48 | ||||
| chr8:100309884-100310170 | Rare:90 | ||||
| chr8:100951257-100951420 | Rare:57 | ||||
| chr8:100951465-100951548 | Common:1; Rare:33 | ||||
| chr8:100953302-100953413 | Common:1; Rare:21 |