| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75289380-75289630 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75393717-75394066 | Common:1; Rare:82 | ||||
| chr17:75456465-75456656 | Rare:51 | ||||
| chr17:75509877-75510123 | Common:2; Rare:41 | ||||
| chr17:75515437-75515640 | Common:3; Rare:61 | ||||
| chr17:75667144-75667470 | Common:5; Rare:109 | ||||
| chr17:75779213-75779538 | Common:1; Rare:166 | ||||
| chr17:75784558-75784872 | Common:2; Rare:138 | ||||
| chr17:75844358-75844537 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:75855276-75855714 | Common:2; Rare:122 | ||||
| chr17:75878552-75878702 | Common:3; Rare:57 | ||||
| chr17:75941023-75941309 | Common:2; Rare:85 | ||||
| chr17:75978618-75978931 | Common:4; Rare:86; Clinvar (pathogenic):1 | ||||
| chr17:75978963-75979283 | Rare:90; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:75979386-75979478 | Common:1; Rare:25; Clinvar (benign):1 |