| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58007114-58007374 | Common:1; Rare:119 | ||||
| chr17:58219216-58219372 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:58328732-58328952 | Common:1; Rare:55 | ||||
| chr17:58692556-58692650 | Common:1; Rare:51; Clinvar:5; Clinvar (benign):16 | ||||
| chr17:59106659-59107070 | Common:3; Rare:134; Clinvar:6; Clinvar (benign):4 | ||||
| chr17:59155150-59155448 | Common:2; Rare:72 | ||||
| chr17:59220394-59220600 | Common:3; Rare:60 | ||||
| chr17:59331486-59331771 | Common:2; Rare:92 | ||||
| chr17:59619557-59619975 | Common:3; Rare:149 | ||||
| chr17:59707402-59707722 | Common:3; Rare:88; Clinvar (benign):2 | ||||
| chr17:59892863-59893170 | Common:1; Rare:92 | ||||
| chr17:59964706-59965088 | Common:2; Rare:117 | ||||
| chr17:60078910-60078976 | Common:4; Rare:35 | ||||
| chr17:60392352-60392447 | Common:2; Rare:29 | ||||
| chr17:60525924-60526283 | Common:2; Rare:118 |