| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:26860460-26860861 | Common:8; Rare:219 | ||||
| chr10:26860800-26861402 | Common:19; Rare:374 | ||||
| chr10:26861523-26861923 | Rare:66 | ||||
| chr10:27099778-27100737 | Common:18; Rare:525; Clinvar:26; Clinvar (benign):13 | ||||
| chr10:27153650-27154040 | Common:4; Rare:104 | ||||
| chr10:27154180-27154600 | Rare:395 | ||||
| chr10:27154752-27155504 | Common:43; Rare:792; Clinvar:32; Clinvar (benign):44 | ||||
| chr10:27155868-27156268 | Common:9; Rare:87 | ||||
| chr10:27240060-27240390 | Common:1; Rare:77 | ||||
| chr10:27240335-27241060 | Common:22; Rare:864 | ||||
| chr10:27241092-27241492 | Common:2; Rare:88 | ||||
| chr10:27241800-27242656 | Common:13; Rare:938 | ||||
| chr10:27503987-27505485 | Common:11; Rare:1336; Clinvar:21; Clinvar (benign):4 | ||||
| chr10:28531840-28532890 | Common:29; Rare:1043 | ||||
| chr10:28532894-28533394 | Common:4; Rare:797 |