| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:88991285-88991438 | Common:2; Rare:30 | ||||
| chr10:92291002-92291521 | Common:6; Rare:165 | ||||
| chr10:92592932-92593162 | Common:3; Rare:69 | ||||
| chr10:92689718-92689989 | Common:3; Rare:93 | ||||
| chr10:93482198-93482467 | Common:2; Rare:70 | ||||
| chr10:95290913-95291159 | Common:2; Rare:100 | ||||
| chr10:95907837-95907916 | Rare:20 | ||||
| chr10:97426044-97426256 | Common:2; Rare:81 | ||||
| chr10:97445987-97446232 | Rare:62 | ||||
| chr10:97498613-97499016 | Common:2; Rare:117 | ||||
| chr10:98446265-98446375 | Rare:14 | ||||
| chr10:99659247-99659542 | Common:1; Rare:75 | ||||
| chr10:99732076-99732329 | Rare:93; Clinvar:3 | ||||
| chr10:100185928-100186089 | Rare:65 | ||||
| chr10:100987409-100987574 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 |