| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:99359472-99359583 | Common:1; Rare:15 | ||||
| chr10:99410941-99411055 | Common:1; Rare:18 | ||||
| chr10:99431383-99431406 | Rare:6 | ||||
| chr10:99622722-99622977 | Rare:50 | ||||
| chr10:100164042-100164168 | Rare:23 | ||||
| chr10:100360445-100360893 | Common:4; Rare:102 | ||||
| chr10:100950610-100950752 | Rare:39 | ||||
| chr10:100989245-100989371 | Common:1; Rare:31; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):6 | ||||
| chr10:101060723-101061124 | Common:2; Rare:103 | ||||
| chr10:101457225-101457312 | Rare:12 | ||||
| chr10:101693801-101693915 | Common:1; Rare:17 | ||||
| chr10:101694399-101694465 | Rare:24 | ||||
| chr10:101767010-101767125 | Common:2; Rare:15 | ||||
| chr10:102121398-102121450 | Rare:4 | ||||
| chr10:102363139-102363330 | Rare:55 |