| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:92574000-92574110 | Common:1; Rare:38 | ||||
| chr10:92592972-92593169 | Common:3; Rare:60 | ||||
| chr10:94362892-94363043 | Common:3; Rare:61 | ||||
| chr10:94545714-94545888 | Common:3; Rare:62 | ||||
| chr10:95290922-95291170 | Common:2; Rare:101 | ||||
| chr10:95693879-95694207 | Common:5; Rare:106; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr10:95907850-95907938 | Common:1; Rare:25 | ||||
| chr10:97426035-97426294 | Common:2; Rare:110 | ||||
| chr10:97445975-97446181 | Rare:54 | ||||
| chr10:97498387-97498550 | Common:2; Rare:64 | ||||
| chr10:98446885-98447247 | Common:1; Rare:80 | ||||
| chr10:99430602-99430957 | Common:3; Rare:87 | ||||
| chr10:99659271-99659571 | Common:2; Rare:75 | ||||
| chr10:99732075-99732361 | Rare:105; Clinvar:4 | ||||
| chr10:100185914-100186088 | Rare:70 |