| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123072452-123072756 | Common:1; Rare:72 | ||||
| chr8:123274178-123274321 | Rare:23 | ||||
| chr8:123274433-123274724 | Common:2; Rare:95 | ||||
| chr8:123416336-123416862 | Common:1; Rare:134 | ||||
| chr8:124372652-124372823 | Common:2; Rare:71 | ||||
| chr8:124474526-124474727 | Rare:77 | ||||
| chr8:124474953-124475260 | Rare:112 | ||||
| chr8:124539022-124539287 | Common:2; Rare:131; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124728396-124728767 | Common:5; Rare:113 | ||||
| chr8:124998176-124998646 | Common:4; Rare:190 | ||||
| chr8:125091626-125091914 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:126558346-126558628 | Common:1; Rare:104 | ||||
| chr8:127735804-127736073 | Common:1; Rare:58 | ||||
| chr8:127736102-127736263 | Common:3; Rare:30 | ||||
| chr8:129939622-129940109 | Common:1; Rare:167 |