| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58488723-58488949 | Common:1; Rare:36 | ||||
| chr17:58514195-58514381 | Rare:40 | ||||
| chr17:58514553-58514793 | Rare:56 | ||||
| chr17:58517788-58518397 | Common:1; Rare:135 | ||||
| chr17:58532023-58532138 | Rare:29 | ||||
| chr17:58692013-58692167 | Common:4; Rare:71 | ||||
| chr17:58692486-58692890 | Common:3; Rare:192; Clinvar:36; Clinvar (benign):34; Clinvar (pathogenic):3 | ||||
| chr17:59106453-59106661 | Rare:58; Clinvar:1 | ||||
| chr17:59106675-59107337 | Common:5; Rare:197; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:59107384-59107508 | Rare:28 | ||||
| chr17:59154656-59155012 | Common:1; Rare:93 | ||||
| chr17:59155113-59155357 | Common:1; Rare:67 | ||||
| chr17:59155531-59155849 | Rare:78 | ||||
| chr17:59209920-59210119 | Common:1; Rare:73 | ||||
| chr17:59220366-59220754 | Common:4; Rare:115 |