| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:93600389-93600686 | Common:6; Rare:167 | ||||
| chr10:95539607-95540225 | Common:7; Rare:145 | ||||
| chr10:95635230-95635750 | Rare:158 | ||||
| chr10:96089758-96090110 | Common:1; Rare:121 | ||||
| chr10:96090179-96090304 | Common:2; Rare:99 | ||||
| chr10:96093230-96093620 | Common:5; Rare:67 | ||||
| chr10:96124351-96124909 | Common:1; Rare:223 | ||||
| chr10:96673392-96673650 | Common:2; Rare:87 | ||||
| chr10:96673730-96674150 | Common:8; Rare:93 | ||||
| chr10:96676580-96676810 | Common:7; Rare:47 | ||||
| chr10:97333170-97333590 | Rare:136 | ||||
| chr10:99329720-99330050 | Common:2; Rare:145 | ||||
| chr10:99779447-99779609 | Common:4; Rare:47 | ||||
| chr10:99803800-99804260 | Common:5; Rare:177; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr10:100342190-100342900 | Common:6; Rare:170 |