| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101587977-101588380 | Rare:149; Clinvar:1 | ||||
| chr10:101694826-101695328 | Common:1; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:101782932-101783034 | Rare:32 | ||||
| chr10:101783050-101783080 | Rare:6 | ||||
| chr10:101783326-101783515 | Rare:82 | ||||
| chr10:101817513-101817543 | Rare:6 | ||||
| chr10:101818306-101818978 | Common:2; Rare:165 | ||||
| chr10:102055763-102055883 | Rare:33 | ||||
| chr10:102055885-102056052 | Common:1; Rare:47 | ||||
| chr10:102056054-102056406 | Common:3; Rare:88 | ||||
| chr10:102065204-102065532 | Common:1; Rare:128 | ||||
| chr10:102065712-102065880 | Common:2; Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:102114264-102114525 | Common:2; Rare:66 | ||||
| chr10:102114527-102114581 | Rare:16 | ||||
| chr10:102114879-102115149 | Common:3; Rare:73 |