| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94719772-94720004 | Common:1; Rare:75 | ||||
| chr8:94895197-94895360 | Rare:50 | ||||
| chr8:94895643-94895802 | Rare:46 | ||||
| chr8:95024779-95025190 | Common:2; Rare:138; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:96235510-96235672 | Common:1; Rare:87; Clinvar (benign):2 | ||||
| chr8:96261566-96261981 | Common:6; Rare:137 | ||||
| chr8:96493825-96494200 | Common:4; Rare:103 | ||||
| chr8:97277876-97278021 | Rare:51 | ||||
| chr8:97775724-97776004 | Common:4; Rare:142; Clinvar (benign):1 | ||||
| chr8:97868767-97869120 | Common:1; Rare:72 | ||||
| chr8:98045345-98045672 | Common:3; Rare:98 | ||||
| chr8:98064452-98064600 | Rare:41 | ||||
| chr8:98117089-98117325 | Common:2; Rare:85 | ||||
| chr8:99013000-99013350 | Rare:72; Clinvar:1 | ||||
| chr8:100105941-100106115 | Rare:49 |