| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:75401382-75401509 | Rare:50 | ||||
| chr10:75401701-75401920 | Common:2; Rare:75 | ||||
| chr10:75402348-75402505 | Common:1; Rare:51 | ||||
| chr10:77637448-77637481 | Rare:12; Clinvar:2 | ||||
| chr10:77926726-77926782 | Rare:12 | ||||
| chr10:78029362-78029605 | Rare:76; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr10:78033580-78033925 | Common:2; Rare:119; Clinvar (benign):4 | ||||
| chr10:79445617-79445934 | Rare:93 | ||||
| chr10:80078608-80078715 | Rare:42 | ||||
| chr10:80078958-80079359 | Common:4; Rare:141 | ||||
| chr10:80157650-80157983 | Common:4; Rare:98 | ||||
| chr10:80453900-80454397 | Common:4; Rare:166 | ||||
| chr10:84139304-84139604 | Common:4; Rare:82 | ||||
| chr10:84424912-84424986 | Rare:18 | ||||
| chr10:86521734-86521974 | Rare:81 |