| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:41650814-41650970 | Common:2; Rare:29 | ||||
| chr8:41797524-41797843 | Common:4; Rare:145; Clinvar (pathogenic):4 | ||||
| chr8:41798084-41798233 | Common:4; Rare:72 | ||||
| chr8:42051962-42052275 | Common:2; Rare:173 | ||||
| chr8:42052330-42052630 | Common:4; Rare:128 | ||||
| chr8:42152650-42153180 | Common:9; Rare:228 | ||||
| chr8:42179620-42180360 | Common:9; Rare:440 | ||||
| chr8:42271243-42271410 | Rare:55 | ||||
| chr8:42338360-42338539 | Common:2; Rare:120 | ||||
| chr8:42391523-42391929 | Common:5; Rare:169 | ||||
| chr8:42541451-42541854 | Common:4; Rare:214 | ||||
| chr8:42542110-42542290 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:42842669-42843060 | Common:5; Rare:178; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:42843278-42843509 | Common:4; Rare:109; Clinvar (benign):6 | ||||
| chr8:42896295-42896513 | Common:2; Rare:117 |