| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:97498694-97499082 | Common:2; Rare:114 | ||||
| chr10:97687309-97687663 | Common:3; Rare:107 | ||||
| chr10:97736974-97737212 | Common:1; Rare:80 | ||||
| chr10:98446539-98446684 | Common:4; Rare:24 | ||||
| chr10:98446850-98447053 | Rare:61; Clinvar:1 | ||||
| chr10:99430616-99430965 | Common:3; Rare:85 | ||||
| chr10:99659219-99659574 | Common:2; Rare:92 | ||||
| chr10:99732043-99732335 | Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:100185757-100186198 | Rare:147 | ||||
| chr10:100229528-100229689 | Rare:63 | ||||
| chr10:100267616-100267721 | Common:2; Rare:36 | ||||
| chr10:100286177-100286459 | Rare:62 | ||||
| chr10:100286623-100286763 | Common:3; Rare:78 | ||||
| chr10:100346921-100347531 | Common:4; Rare:145 | ||||
| chr10:100529831-100530010 | Common:1; Rare:48 |