| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123274427-123274711 | Common:2; Rare:94 | ||||
| chr8:123396191-123396307 | Rare:49 | ||||
| chr8:123396311-123396525 | Common:1; Rare:104 | ||||
| chr8:123416302-123416852 | Common:1; Rare:145 | ||||
| chr8:123416908-123416975 | Rare:24 | ||||
| chr8:123532115-123532274 | Common:2; Rare:22 | ||||
| chr8:124450773-124450842 | Rare:27 | ||||
| chr8:124451318-124451500 | Rare:59 | ||||
| chr8:124474521-124474784 | Common:1; Rare:98 | ||||
| chr8:124474941-124475249 | Rare:108 | ||||
| chr8:124538418-124538643 | Common:2; Rare:47 | ||||
| chr8:124538981-124539292 | Common:2; Rare:158; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124728396-124728608 | Rare:61 | ||||
| chr8:124998182-124998710 | Common:5; Rare:207 | ||||
| chr8:125091709-125091930 | Common:2; Rare:77; Clinvar (benign):3 |