| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:61056880-61057310 | Common:1; Rare:101 | ||||
| chr8:61714504-61714990 | Common:2; Rare:138 | ||||
| chr8:63038734-63038981 | Common:3; Rare:89 | ||||
| chr8:63039090-63039350 | Common:3; Rare:41 | ||||
| chr8:63039431-63039573 | Common:1; Rare:38 | ||||
| chr8:63085541-63086514 | Common:16; Rare:359; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
| chr8:63168307-63168661 | Common:2; Rare:120 | ||||
| chr8:64579791-64580191 | Rare:109 | ||||
| chr8:64798530-64798940 | Common:4; Rare:119; Clinvar:8; Clinvar (benign):3 | ||||
| chr8:65634096-65634462 | Common:4; Rare:98 | ||||
| chr8:65644516-65644842 | Common:4; Rare:84 | ||||
| chr8:65840963-65841392 | Common:1; Rare:142 | ||||
| chr8:65841316-65841779 | Common:2; Rare:175 | ||||
| chr8:65841932-65842173 | Common:2; Rare:102 | ||||
| chr8:65842458-65842754 | Common:2; Rare:86 |