| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:57256083-57256234 | Common:2; Rare:20 | ||||
| chr17:57256284-57256661 | Common:1; Rare:80 | ||||
| chr17:57285371-57285498 | Common:1; Rare:28 | ||||
| chr17:57849984-57850370 | Common:1; Rare:122 | ||||
| chr17:57850448-57850601 | Rare:31 | ||||
| chr17:57868172-57868280 | Common:1; Rare:33 | ||||
| chr17:57903297-57903455 | Rare:22 | ||||
| chr17:57988154-57988607 | Common:5; Rare:141 | ||||
| chr17:58007114-58007515 | Common:1; Rare:170 | ||||
| chr17:58007526-58007838 | Common:1; Rare:67 | ||||
| chr17:58083147-58083463 | Common:4; Rare:118 | ||||
| chr17:58219140-58219469 | Common:2; Rare:125; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:58249573-58249889 | Common:1; Rare:95 | ||||
| chr17:58352116-58352514 | Common:6; Rare:144 | ||||
| chr17:58353026-58353170 | Common:1; Rare:28 |