| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7012317-7012732 | Rare:134 | ||||
| chr17:7022861-7023104 | Common:3; Rare:57 | ||||
| chr17:7219728-7219990 | Common:3; Rare:103; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:7223976-7224206 | Rare:81; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):9 | ||||
| chr17:7224318-7224846 | Common:4; Rare:194; Clinvar:13; Clinvar (benign):23; Clinvar (pathogenic):4 | ||||
| chr17:7241778-7242148 | Common:3; Rare:82 | ||||
| chr17:7242171-7242595 | Common:2; Rare:135 | ||||
| chr17:7251963-7252321 | Common:1; Rare:141 | ||||
| chr17:7281385-7281771 | Common:2; Rare:100 | ||||
| chr17:7307260-7307707 | Common:6; Rare:129 | ||||
| chr17:7313413-7313621 | Common:1; Rare:90 | ||||
| chr17:7315069-7315440 | Common:4; Rare:129 | ||||
| chr17:7350267-7350370 | Common:2; Rare:34 | ||||
| chr17:7352041-7352207 | Rare:55 | ||||
| chr17:7404076-7404332 | Common:1; Rare:74 |