| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:120812424-120812707 | Rare:58 | ||||
| chr8:122781234-122781585 | Common:1; Rare:73 | ||||
| chr8:122781599-122781940 | Common:3; Rare:67 | ||||
| chr8:123042166-123042367 | Common:1; Rare:59 | ||||
| chr8:123273927-123274320 | Common:1; Rare:76 | ||||
| chr8:123274376-123274747 | Common:2; Rare:110 | ||||
| chr8:123396197-123396562 | Common:2; Rare:164 | ||||
| chr8:123416388-123416842 | Common:1; Rare:115 | ||||
| chr8:124372659-124372796 | Common:2; Rare:58 | ||||
| chr8:124474521-124474778 | Common:1; Rare:95 | ||||
| chr8:124474935-124475148 | Rare:70 | ||||
| chr8:124538981-124539304 | Common:2; Rare:160; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091626-125091938 | Common:2; Rare:104; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:125430241-125430432 | Common:1; Rare:47 | ||||
| chr8:125430457-125430481 | Rare:3 |