| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:110871695-110872010 | Rare:106 | ||||
| chr10:110872170-110872616 | Common:1; Rare:138 | ||||
| chr10:110918492-110918831 | Common:3; Rare:99 | ||||
| chr10:110918859-110918954 | Common:1; Rare:31 | ||||
| chr10:110919088-110919700 | Common:8; Rare:168; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:110919715-110919824 | Rare:36 | ||||
| chr10:112183639-112183984 | Common:3; Rare:115 | ||||
| chr10:112375092-112375365 | Common:2; Rare:45 | ||||
| chr10:112375934-112376429 | Rare:103 | ||||
| chr10:112376571-112376676 | Common:2; Rare:23 | ||||
| chr10:112446832-112447384 | Common:3; Rare:145 | ||||
| chr10:113679156-113679286 | Rare:31 | ||||
| chr10:113679525-113680078 | Common:5; Rare:166 | ||||
| chr10:113854013-113854697 | Rare:144 | ||||
| chr10:113854834-113854957 | Rare:37 |