| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94553430-94553749 | Common:3; Rare:115 | ||||
| chr8:94719772-94719960 | Common:1; Rare:54 | ||||
| chr8:94895178-94895324 | Rare:51 | ||||
| chr8:94895643-94895806 | Rare:47 | ||||
| chr8:94949316-94949520 | Common:2; Rare:61 | ||||
| chr8:95024945-95025195 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:95268560-95268844 | Common:8; Rare:64 | ||||
| chr8:96235510-96235657 | Common:1; Rare:77; Clinvar (benign):2 | ||||
| chr8:96261566-96261977 | Common:6; Rare:136 | ||||
| chr8:96493748-96493854 | Rare:36 | ||||
| chr8:96494003-96494330 | Common:3; Rare:103 | ||||
| chr8:97277897-97277924 | Rare:12 | ||||
| chr8:97643844-97644237 | Common:9; Rare:98 | ||||
| chr8:97644647-97644854 | Common:1; Rare:71 | ||||
| chr8:98045327-98045618 | Common:3; Rare:90 |