| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44221560-44221790 | Common:4; Rare:66 | ||||
| chr17:44268064-44269297 | Common:3; Rare:365; Clinvar:7 | ||||
| chr17:44324695-44325095 | Common:22; Rare:707 | ||||
| chr17:44325160-44325520 | Common:8; Rare:131 | ||||
| chr17:44344972-44345430 | Common:5; Rare:230; Clinvar:15; Clinvar (benign):11 | ||||
| chr17:44362930-44363850 | Common:3; Rare:198 | ||||
| chr17:44385246-44385732 | Common:25; Rare:697; Clinvar:13 | ||||
| chr17:44389255-44390160 | Common:6; Rare:506; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:44502538-44502938 | Common:3; Rare:91 | ||||
| chr17:44503110-44503940 | Common:2; Rare:1134 | ||||
| chr17:44557000-44557678 | Common:6; Rare:370 | ||||
| chr17:44689379-44690130 | Common:3; Rare:428 | ||||
| chr17:44690248-44690648 | Common:2; Rare:85 | ||||
| chr17:44708290-44709488 | Common:25; Rare:629 | ||||
| chr17:44775612-44776012 | Common:14; Rare:246 |