| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94553440-94553769 | Common:3; Rare:117 | ||||
| chr8:94719730-94719960 | Common:1; Rare:64 | ||||
| chr8:94823145-94823343 | Common:2; Rare:69 | ||||
| chr8:94895175-94895342 | Rare:57 | ||||
| chr8:94895643-94895864 | Common:3; Rare:63 | ||||
| chr8:94896630-94896746 | Common:3; Rare:30 | ||||
| chr8:95024779-95025184 | Common:2; Rare:138; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:95268718-95268864 | Common:8; Rare:37 | ||||
| chr8:95269198-95269320 | Common:5; Rare:48; Clinvar:1 | ||||
| chr8:95269374-95269675 | Common:7; Rare:102 | ||||
| chr8:96235510-96235662 | Common:1; Rare:79; Clinvar (benign):2 | ||||
| chr8:96261553-96261957 | Common:6; Rare:139 | ||||
| chr8:96493518-96493831 | Rare:95 | ||||
| chr8:96494063-96494171 | Common:3; Rare:30 | ||||
| chr8:97775688-97776053 | Common:6; Rare:185; Clinvar (benign):1 |