| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:86971039-86971112 | Rare:14 | ||||
| chr10:86971146-86971196 | Rare:14 | ||||
| chr10:86971202-86971480 | Common:2; Rare:92 | ||||
| chr10:87342273-87342942 | Common:6; Rare:208 | ||||
| chr10:87862320-87862594 | Rare:126; Clinvar:1 | ||||
| chr10:88938049-88938377 | Rare:69; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr10:88939505-88939955 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr10:88948909-88949041 | Rare:28; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr10:89283339-89283691 | Common:1; Rare:54 | ||||
| chr10:91162260-91162403 | Common:1; Rare:20 | ||||
| chr10:91807502-91807537 | Rare:12 | ||||
| chr10:92695958-92696161 | Rare:44 | ||||
| chr10:92699747-92699891 | Common:2; Rare:27 | ||||
| chr10:93468496-93468741 | Common:3; Rare:45 | ||||
| chr10:100346426-100346517 | Common:2; Rare:18 |