| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:12789389-12789540 | Rare:54 | ||||
| chr17:13017188-13017664 | Common:2; Rare:145 | ||||
| chr17:13017937-13018370 | Common:8; Rare:141; Clinvar (benign):2 | ||||
| chr17:13601885-13602186 | Common:3; Rare:93 | ||||
| chr17:13602310-13602730 | Common:4; Rare:101 | ||||
| chr17:14069333-14069593 | Common:2; Rare:94; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:14069713-14070113 | Common:4; Rare:132 | ||||
| chr17:14300770-14301141 | Common:3; Rare:98 | ||||
| chr17:15260259-15260659 | Common:5; Rare:92; Clinvar:1 | ||||
| chr17:15260813-15261587 | Common:6; Rare:208; Clinvar (benign):1 | ||||
| chr17:15563550-15563793 | Common:1; Rare:73 | ||||
| chr17:15651816-15651989 | Rare:24 | ||||
| chr17:15684226-15684334 | Common:3; Rare:38 | ||||
| chr17:15699442-15699771 | Common:4; Rare:88 | ||||
| chr17:15944500-15944900 | Common:5; Rare:109 |