| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:120445087-120445440 | Common:1; Rare:86 | ||||
| chr8:124539042-124539190 | Common:2; Rare:82; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:125091717-125091914 | Common:2; Rare:68; Clinvar (benign):3 | ||||
| chr8:127735911-127736073 | Rare:35 | ||||
| chr8:127736113-127736257 | Common:3; Rare:26 | ||||
| chr8:141001202-141001508 | Common:3; Rare:113 | ||||
| chr8:143018403-143018554 | Common:1; Rare:44 | ||||
| chr8:143558247-143558387 | Common:1; Rare:49 | ||||
| chr8:143829308-143829544 | Rare:99 | ||||
| chr8:144078477-144078722 | Common:1; Rare:75 | ||||
| chr8:145052209-145052494 | Common:10; Rare:82 | ||||
| chr9:2844057-2844320 | Common:4; Rare:97 | ||||
| chr9:4679437-4679677 | Rare:111 | ||||
| chr9:5437824-5438016 | Common:1; Rare:63 | ||||
| chr9:19127424-19127733 | Common:6; Rare:95 |