| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:70164252-70164416 | Common:1; Rare:31 | ||||
| chr10:72190286-72190525 | Rare:38 | ||||
| chr10:72272860-72273085 | Common:1; Rare:53 | ||||
| chr10:72353708-72353795 | Common:1; Rare:17 | ||||
| chr10:73045002-73045178 | Common:2; Rare:53 | ||||
| chr10:73126186-73126209 | Rare:3 | ||||
| chr10:73246800-73246981 | Rare:73 | ||||
| chr10:73247034-73247049 | Common:1; Rare:4 | ||||
| chr10:73247176-73247383 | Rare:117 | ||||
| chr10:73730443-73730617 | Common:1; Rare:43 | ||||
| chr10:73966127-73966377 | Common:1; Rare:43 | ||||
| chr10:74070731-74071055 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):6 | ||||
| chr10:75223634-75223890 | Common:2; Rare:46 | ||||
| chr10:76054742-76054773 | Common:1; Rare:3 | ||||
| chr10:76821398-76821558 | Common:1; Rare:20 |