| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68513343-68513439 | Rare:30 | ||||
| chr17:72120802-72121068 | Rare:70 | ||||
| chr17:73192796-73193126 | Common:15; Rare:136; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:73232100-73232715 | Common:4; Rare:235 | ||||
| chr17:73233037-73233318 | Common:4; Rare:70 | ||||
| chr17:74203568-74203957 | Common:3; Rare:137 | ||||
| chr17:74776235-74776548 | Common:4; Rare:101 | ||||
| chr17:75012593-75012881 | Common:1; Rare:88 | ||||
| chr17:75046926-75047209 | Common:1; Rare:86 | ||||
| chr17:75109854-75110005 | Common:2; Rare:44 | ||||
| chr17:75130765-75131096 | Common:2; Rare:116 | ||||
| chr17:75131602-75132017 | Common:5; Rare:158 | ||||
| chr17:75182833-75183211 | Common:2; Rare:135 | ||||
| chr17:75205376-75205770 | Common:1; Rare:132 | ||||
| chr17:75261568-75262011 | Common:10; Rare:163; Clinvar (benign):4 |