| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:57849981-57850292 | Common:1; Rare:104 | ||||
| chr17:57988115-57988535 | Common:6; Rare:122 | ||||
| chr17:58006588-58006728 | Rare:45 | ||||
| chr17:58007178-58007390 | Common:1; Rare:98 | ||||
| chr17:58007604-58007766 | Rare:41 | ||||
| chr17:58219193-58219387 | Common:1; Rare:79; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:58352125-58352428 | Common:5; Rare:127 | ||||
| chr17:58531976-58532143 | Rare:40 | ||||
| chr17:58692541-58692751 | Common:2; Rare:112; Clinvar:28; Clinvar (benign):27; Clinvar (pathogenic):2 | ||||
| chr17:58755817-58755893 | Rare:24 | ||||
| chr17:59106685-59106977 | Common:2; Rare:98; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:59154979-59155362 | Common:1; Rare:115 | ||||
| chr17:59155404-59155793 | Rare:98 | ||||
| chr17:59220388-59220658 | Common:4; Rare:80 | ||||
| chr17:59565469-59565745 | Common:1; Rare:102 |