| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:82019746-82020146 | Common:6; Rare:177 | ||||
| chr17:82092265-82092951 | Common:16; Rare:463; Clinvar:17; Clinvar (benign):20 | ||||
| chr17:82093012-82093308 | Common:4; Rare:103; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:82093270-82093670 | Common:5; Rare:217; Clinvar:3; Clinvar (benign):5 | ||||
| chr17:82104251-82104580 | Common:5; Rare:116 | ||||
| chr17:82149160-82149930 | Common:11; Rare:131 | ||||
| chr17:82217590-82218050 | Common:4; Rare:180 | ||||
| chr17:82230863-82231270 | Common:2; Rare:251 | ||||
| chr17:82265720-82265980 | Rare:62; Clinvar (pathogenic):1 | ||||
| chr17:82292750-82292988 | Common:9; Rare:132 | ||||
| chr17:82325341-82325695 | Common:2; Rare:101 | ||||
| chr17:82346351-82346753 | Common:3; Rare:141 | ||||
| chr17:82349370-82349720 | Common:3; Rare:116 | ||||
| chr17:82495798-82496198 | Common:7; Rare:140 | ||||
| chr17:82517330-82517690 | Rare:115 |