| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73743996-73744430 | Common:1; Rare:109 | ||||
| chr10:73772214-73772330 | Common:2; Rare:51 | ||||
| chr10:73772643-73772870 | Rare:110 | ||||
| chr10:73781957-73782332 | Common:1; Rare:120 | ||||
| chr10:73793708-73793996 | Rare:78 | ||||
| chr10:73800125-73800335 | Rare:72 | ||||
| chr10:73874473-73874760 | Rare:76 | ||||
| chr10:74104827-74105142 | Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:74151042-74151281 | Common:1; Rare:74 | ||||
| chr10:74176609-74176831 | Rare:58; Clinvar:3 | ||||
| chr10:74826106-74826431 | Common:2; Rare:84 | ||||
| chr10:75109180-75109349 | Rare:28 | ||||
| chr10:75111428-75111707 | Common:1; Rare:79 | ||||
| chr10:75210433-75210867 | Common:1; Rare:154 | ||||
| chr10:77637369-77637508 | Common:1; Rare:35; Clinvar:3; Clinvar (benign):1 |