| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73495807-73496130 | Common:2; Rare:90 | ||||
| chr10:73625953-73626117 | Rare:30 | ||||
| chr10:73743857-73744440 | Common:2; Rare:139 | ||||
| chr10:73744771-73744896 | Rare:22 | ||||
| chr10:73772092-73772334 | Common:3; Rare:75 | ||||
| chr10:73772972-73773174 | Common:1; Rare:63 | ||||
| chr10:73781945-73782439 | Common:1; Rare:155 | ||||
| chr10:73874440-73874723 | Rare:73 | ||||
| chr10:73909141-73909452 | Common:2; Rare:43 | ||||
| chr10:73997732-73998516 | Common:2; Rare:193; Clinvar:4; Clinvar (benign):6 | ||||
| chr10:74105209-74105476 | Common:3; Rare:75; Clinvar:5; Clinvar (benign):5 | ||||
| chr10:74150750-74151251 | Common:3; Rare:115 | ||||
| chr10:74176695-74176862 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:74826314-74826611 | Common:2; Rare:73; Clinvar (benign):2 | ||||
| chr10:75210259-75210854 | Common:3; Rare:190 |