| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58692501-58692674 | Common:2; Rare:95; Clinvar:13; Clinvar (benign):20 | ||||
| chr17:59106872-59106970 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:59155162-59155761 | Common:2; Rare:146 | ||||
| chr17:59619805-59620164 | Common:1; Rare:121 | ||||
| chr17:59707379-59707745 | Common:4; Rare:102; Clinvar (benign):6 | ||||
| chr17:59892715-59893140 | Rare:113 | ||||
| chr17:59964719-59965060 | Common:2; Rare:100 | ||||
| chr17:60078913-60078993 | Common:4; Rare:38 | ||||
| chr17:60525920-60526334 | Common:2; Rare:148 | ||||
| chr17:61399514-61399926 | Common:1; Rare:113 | ||||
| chr17:61863457-61863675 | Common:1; Rare:42; Clinvar:2 | ||||
| chr17:63550238-63550532 | Common:1; Rare:71 | ||||
| chr17:63699738-63700293 | Common:2; Rare:140 | ||||
| chr17:63700694-63700856 | Common:3; Rare:51 | ||||
| chr17:63741764-63741952 | Common:3; Rare:71 |