| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17228916-17229026 | Common:1; Rare:29 | ||||
| chr10:17229129-17229212 | Common:1; Rare:13 | ||||
| chr10:17230554-17230710 | Rare:68; Clinvar:1 | ||||
| chr10:17233558-17233928 | Common:2; Rare:116; Clinvar (benign):1 | ||||
| chr10:17643871-17644306 | Common:2; Rare:133 | ||||
| chr10:18140610-18140899 | Common:2; Rare:109; Clinvar:5; Clinvar (benign):9 | ||||
| chr10:18140936-18141114 | Common:2; Rare:36 | ||||
| chr10:18141137-18141188 | Rare:15 | ||||
| chr10:18651564-18651733 | Common:1; Rare:70 | ||||
| chr10:18659254-18659414 | Common:2; Rare:52 | ||||
| chr10:19816076-19816282 | Common:2; Rare:54 | ||||
| chr10:19816305-19816653 | Common:5; Rare:75 | ||||
| chr10:21526404-21526568 | Common:1; Rare:53 | ||||
| chr10:21533939-21534314 | Common:2; Rare:145 | ||||
| chr10:22316258-22316514 | Common:1; Rare:118 |