| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:13017924-13018370 | Common:8; Rare:147; Clinvar (benign):2 | ||||
| chr17:14069333-14069593 | Common:2; Rare:94; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:14069979-14070013 | Rare:10 | ||||
| chr17:14300773-14301148 | Common:3; Rare:99 | ||||
| chr17:15262550-15262714 | Rare:39 | ||||
| chr17:15341591-15341711 | Common:2; Rare:26 | ||||
| chr17:15563418-15563784 | Common:1; Rare:125 | ||||
| chr17:15651596-15651995 | Common:1; Rare:78 | ||||
| chr17:15684228-15684324 | Common:3; Rare:35 | ||||
| chr17:15699446-15699823 | Common:5; Rare:108 | ||||
| chr17:15944940-15945152 | Rare:51 | ||||
| chr17:15945175-15945315 | Common:2; Rare:36 | ||||
| chr17:15999523-15999877 | Common:3; Rare:178; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr17:16214973-16215140 | Rare:50 | ||||
| chr17:16215463-16215741 | Common:3; Rare:127 |