| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:99905434-99905733 | Not yet | Common:2; Rare:43 | 385 | ||
| chr10:99923665-99923912 | Not yet | Common:3; Rare:42 | 314 | ||
| chr10:99927022-99927302 | Not yet | Common:2; Rare:51 | 353 | ||
| chr10:99930792-99931029 | Not yet | Common:2; Rare:61 | 324 | ||
| chr10:100236169-100236173 | Not yet | 1 | |||
| chr10:100970112-100970382 | Not yet | Rare:68 | 271 | ||
| chr10:100979618-100979882 | Not yet | Common:1; Rare:64 | 276 | ||
| chr10:101032195-101032457 | Not yet | Common:3; Rare:61 | 296 | ||
| chr10:101694404-101694693 | Not yet | Common:4; Rare:93; Clinvar:3; Clinvar (benign):5 | 194 | ||
| chr10:102109451-102109605 | Not yet | Common:1; Rare:31 | 223 | ||
| chr10:102363067-102363322 | Not yet | Common:1; Rare:61 | 281 | ||
| chr10:102919642-102920095 | Not yet | Rare:82; Clinvar:1 | 383 | ||
| chr10:103090721-103091040 | Not yet | Common:5; Rare:86; Clinvar (pathogenic):1 | 385 | ||
| chr10:103097296-103097647 | Not yet | Common:3; Rare:64 | 390 | ||
| chr10:103192445-103192679 | Not yet | Rare:59 | 311 |