| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12882040-12882145 | Rare:18 | ||||
| chr10:13118341-13119070 | Common:5; Rare:231; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:13158371-13158547 | Common:5; Rare:54 | ||||
| chr10:13158625-13158848 | Common:3; Rare:63 | ||||
| chr10:13349062-13349242 | Rare:47 | ||||
| chr10:13382580-13383262 | Common:4; Rare:241 | ||||
| chr10:13399630-13400885 | Common:10; Rare:428 | ||||
| chr10:13404697-13405125 | Common:8; Rare:197 | ||||
| chr10:13409720-13410380 | Common:5; Rare:142 | ||||
| chr10:13717947-13718151 | Common:4; Rare:40 | ||||
| chr10:13990316-13990733 | Common:7; Rare:177 | ||||
| chr10:14074470-14074790 | Common:2; Rare:68 | ||||
| chr10:14153648-14154023 | Common:4; Rare:84 | ||||
| chr10:14407520-14407980 | Common:1; Rare:103 | ||||
| chr10:14647989-14648598 | Common:9; Rare:207 |