| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:96129932-96130580 | Common:5; Rare:222 | ||||
| chr10:97426034-97426317 | Common:2; Rare:131 | ||||
| chr10:97445894-97446226 | Common:2; Rare:103 | ||||
| chr10:97498376-97498550 | Common:2; Rare:73 | ||||
| chr10:97498802-97499153 | Rare:98 | ||||
| chr10:97633436-97633671 | Common:2; Rare:63 | ||||
| chr10:97687233-97687507 | Common:4; Rare:88 | ||||
| chr10:97736939-97737212 | Common:2; Rare:93 | ||||
| chr10:98134537-98134695 | Common:1; Rare:57 | ||||
| chr10:98446182-98446378 | Common:1; Rare:40 | ||||
| chr10:98446826-98446947 | Rare:34; Clinvar:1 | ||||
| chr10:99430513-99430940 | Common:4; Rare:109 | ||||
| chr10:99659245-99659536 | Common:1; Rare:74 | ||||
| chr10:99732028-99732339 | Rare:117; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:100185938-100186230 | Rare:108 |