| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:110225838-110226213 | Common:2; Rare:100 | ||||
| chr10:110304890-110304975 | Common:2; Rare:39 | ||||
| chr10:110871622-110872016 | Rare:135 | ||||
| chr10:110872151-110872235 | Rare:21 | ||||
| chr10:110872246-110872588 | Common:1; Rare:114 | ||||
| chr10:110919285-110919654 | Common:7; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:112183712-112183844 | Common:2; Rare:51 | ||||
| chr10:112374015-112374259 | Rare:34 | ||||
| chr10:112374801-112375269 | Common:4; Rare:84 | ||||
| chr10:112422165-112422441 | Rare:77 | ||||
| chr10:112446832-112447441 | Common:4; Rare:167 | ||||
| chr10:112950002-112950380 | Common:3; Rare:86 | ||||
| chr10:112950387-112950922 | Common:6; Rare:105 | ||||
| chr10:112950935-112951270 | Common:2; Rare:85 | ||||
| chr10:113152156-113152358 | Common:1; Rare:35 |