| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42391741-42391917 | Common:2; Rare:63 | ||||
| chr8:42501130-42501560 | Common:2; Rare:87 | ||||
| chr8:42541557-42541846 | Rare:106 | ||||
| chr8:42542049-42542154 | Common:1; Rare:25; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:42842739-42843090 | Common:2; Rare:104; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:42843260-42843575 | Common:3; Rare:86; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:42895842-42896360 | Common:3; Rare:267 | ||||
| chr8:42896591-42897027 | Common:1; Rare:177 | ||||
| chr8:42897154-42897554 | Common:5; Rare:152 | ||||
| chr8:43056005-43056372 | Common:2; Rare:110 | ||||
| chr8:43056500-43056730 | Rare:72 | ||||
| chr8:43093414-43093562 | Common:3; Rare:30; Clinvar (benign):1 | ||||
| chr8:43140238-43140529 | Common:2; Rare:117; Clinvar:6 | ||||
| chr8:47260721-47260991 | Common:3; Rare:122 | ||||
| chr8:47659414-47659949 | Common:2; Rare:192 |