| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124474521-124474778 | Common:1; Rare:95 | ||||
| chr8:124474946-124475112 | Rare:54 | ||||
| chr8:124539037-124539293 | Common:2; Rare:124; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124546717-124547075 | Common:1; Rare:67; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:124549872-124550150 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr8:124728376-124728582 | Rare:60 | ||||
| chr8:124998164-124998778 | Common:5; Rare:224 | ||||
| chr8:124998980-124999296 | Common:4; Rare:79 | ||||
| chr8:125091626-125091914 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:126557652-126557907 | Rare:61 | ||||
| chr8:126558269-126558638 | Common:1; Rare:129 | ||||
| chr8:127735864-127736116 | Rare:53 | ||||
| chr8:127736119-127736527 | Common:4; Rare:104 | ||||
| chr8:129939731-129939874 | Common:1; Rare:51 | ||||
| chr8:130016379-130016760 | Common:3; Rare:109 |