| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73495611-73495755 | Rare:28 | ||||
| chr10:73495773-73496154 | Common:3; Rare:110 | ||||
| chr10:73625834-73626109 | Rare:57 | ||||
| chr10:73744252-73744442 | Common:1; Rare:51 | ||||
| chr10:73772625-73773073 | Common:1; Rare:209 | ||||
| chr10:73782005-73782357 | Common:1; Rare:112 | ||||
| chr10:73874461-73874738 | Rare:70 | ||||
| chr10:74150767-74151293 | Common:2; Rare:131 | ||||
| chr10:74176415-74176778 | Rare:91; Clinvar:2 | ||||
| chr10:74825240-74825610 | Rare:96 | ||||
| chr10:75111301-75111769 | Common:1; Rare:134 | ||||
| chr10:75210429-75210886 | Common:2; Rare:161 | ||||
| chr10:75210920-75211026 | Rare:35 | ||||
| chr10:75229575-75229696 | Rare:29 | ||||
| chr10:77637454-77637517 | Common:1; Rare:21; Clinvar:2; Clinvar (benign):1 |