| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76537916-76537957 | Rare:13 | ||||
| chr17:76726484-76726895 | Common:5; Rare:154 | ||||
| chr17:76737325-76737689 | Common:3; Rare:125 | ||||
| chr17:76737892-76738119 | Common:4; Rare:67 | ||||
| chr17:77319832-77319935 | Common:1; Rare:21; Clinvar (benign):1 | ||||
| chr17:78187004-78187364 | Common:3; Rare:123 | ||||
| chr17:78840736-78841060 | Common:2; Rare:118 | ||||
| chr17:79009744-79009917 | Common:8; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:80220364-80220447 | Rare:28 | ||||
| chr17:81239036-81239387 | Common:4; Rare:113 | ||||
| chr17:81512708-81512808 | Common:3; Rare:77; Clinvar (benign):14 | ||||
| chr17:81552378-81552487 | Rare:40 | ||||
| chr17:81666564-81666763 | Common:1; Rare:87 | ||||
| chr17:81683659-81684052 | Common:4; Rare:201 | ||||
| chr17:81703292-81703571 | Common:2; Rare:83; Clinvar (benign):2 |