| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143635977-143636072 | Common:1; Rare:39 | ||||
| chr8:143684328-143684494 | Common:2; Rare:38 | ||||
| chr8:143829033-143829185 | Rare:53 | ||||
| chr8:143829300-143829550 | Rare:108 | ||||
| chr8:143878452-143878629 | Common:4; Rare:59 | ||||
| chr8:143991409-143991747 | Rare:131 | ||||
| chr8:143992469-143992882 | Common:2; Rare:139 | ||||
| chr8:144060674-144060862 | Rare:58 | ||||
| chr8:144078512-144078740 | Common:1; Rare:70 | ||||
| chr8:144082503-144082701 | Common:2; Rare:67 | ||||
| chr8:144096123-144096494 | Common:1; Rare:137; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:144099604-144099708 | Common:1; Rare:32 | ||||
| chr8:144103652-144103868 | Common:1; Rare:73 | ||||
| chr8:144104103-144104530 | Common:4; Rare:154 | ||||
| chr8:144317378-144317523 | Rare:58; Clinvar (pathogenic):1 |