| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:142777776-142777912 | Rare:31 | ||||
| chr8:142785839-142785998 | Rare:26 | ||||
| chr8:142874955-142875382 | Common:4; Rare:169; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):8 | ||||
| chr8:142879506-142880177 | Common:9; Rare:214; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
| chr8:142917829-142917865 | Rare:12; Clinvar (benign):1 | ||||
| chr8:143018371-143018583 | Common:2; Rare:63 | ||||
| chr8:143334787-143334960 | Common:2; Rare:65 | ||||
| chr8:143541424-143541673 | Common:3; Rare:81 | ||||
| chr8:143553509-143553681 | Common:1; Rare:24 | ||||
| chr8:143557997-143558020 | Rare:5 | ||||
| chr8:143558225-143558445 | Common:2; Rare:85 | ||||
| chr8:143580933-143581155 | Common:4; Rare:79 | ||||
| chr8:143597100-143597250 | Common:1; Rare:47 | ||||
| chr8:143635977-143636065 | Common:1; Rare:37 | ||||
| chr8:143684371-143684525 | Common:4; Rare:34 |