| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75393569-75393611 | Rare:6 | ||||
| chr17:75393732-75394123 | Common:1; Rare:86 | ||||
| chr17:75404923-75405159 | Common:1; Rare:56 | ||||
| chr17:75405556-75405781 | Common:1; Rare:76 | ||||
| chr17:75456103-75456228 | Common:1; Rare:28 | ||||
| chr17:75456387-75456761 | Common:3; Rare:116 | ||||
| chr17:75459508-75459738 | Rare:36 | ||||
| chr17:75459966-75460136 | Rare:21 | ||||
| chr17:75514822-75515004 | Common:1; Rare:30 | ||||
| chr17:75515419-75515714 | Common:3; Rare:88 | ||||
| chr17:75516411-75516619 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:75516840-75517231 | Common:5; Rare:170; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr17:75524858-75525057 | Common:1; Rare:55 | ||||
| chr17:75525252-75525778 | Common:4; Rare:142 | ||||
| chr17:75525953-75526018 | Rare:13 |