| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:57903298-57903698 | Common:2; Rare:159 | ||||
| chr17:57955170-57956010 | Common:5; Rare:330 | ||||
| chr17:57985500-57985971 | Common:4; Rare:115 | ||||
| chr17:57987393-57987809 | Common:2; Rare:245 | ||||
| chr17:57987919-57988597 | Common:20; Rare:448 | ||||
| chr17:58006415-58006728 | Common:2; Rare:155 | ||||
| chr17:58006634-58006782 | Rare:47 | ||||
| chr17:58006967-58007461 | Common:3; Rare:484 | ||||
| chr17:58007500-58007929 | Common:4; Rare:211 | ||||
| chr17:58083148-58083562 | Common:16; Rare:397 | ||||
| chr17:58218467-58218889 | Common:3; Rare:195; Clinvar:12; Clinvar (pathogenic):4 | ||||
| chr17:58219151-58219474 | Common:4; Rare:274; Clinvar:14; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr17:58351427-58351827 | Common:1; Rare:91 | ||||
| chr17:58351997-58352563 | Common:18; Rare:480 | ||||
| chr17:58363878-58364016 | Rare:30 |