| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:14953927-14954268 | Rare:248; Clinvar (benign):1 | ||||
| chr10:14954335-14954580 | Common:5; Rare:96 | ||||
| chr10:14959216-14959860 | Common:6; Rare:409 | ||||
| chr10:14959880-14960107 | Common:3; Rare:113 | ||||
| chr10:15088695-15088930 | Common:2; Rare:156 | ||||
| chr10:15097019-15097482 | Common:20; Rare:512 | ||||
| chr10:15168526-15169160 | Common:6; Rare:258 | ||||
| chr10:15860336-15860631 | Common:2; Rare:174 | ||||
| chr10:16436762-16437146 | Common:2; Rare:90 | ||||
| chr10:16817310-16817777 | Common:14; Rare:445 | ||||
| chr10:17201260-17201678 | Common:15; Rare:236 | ||||
| chr10:17201606-17201741 | Common:1; Rare:52 | ||||
| chr10:17229096-17229286 | Common:2; Rare:39 | ||||
| chr10:17229655-17230362 | Common:6; Rare:437; Clinvar (pathogenic):2 | ||||
| chr10:17230451-17230687 | Common:2; Rare:233 |