| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:100722120-100722493 | Common:1; Rare:120 | ||||
| chr8:100722696-100722910 | Rare:75 | ||||
| chr8:100950107-100950225 | Rare:28 | ||||
| chr8:100950418-100950711 | Common:11; Rare:124 | ||||
| chr8:100952461-100952812 | Common:1; Rare:117 | ||||
| chr8:100953301-100953440 | Common:1; Rare:29 | ||||
| chr8:101205495-101205961 | Common:4; Rare:148 | ||||
| chr8:101206142-101206317 | Common:1; Rare:37 | ||||
| chr8:102238654-102239588 | Common:14; Rare:300; Clinvar:1; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:102412689-102412977 | Common:3; Rare:70 | ||||
| chr8:102551526-102551623 | Rare:12 | ||||
| chr8:102655656-102655783 | Common:1; Rare:57 | ||||
| chr8:102863399-102863742 | Common:4; Rare:105 | ||||
| chr8:102863772-102863856 | Rare:14 | ||||
| chr8:102864089-102864562 | Common:6; Rare:188 |