| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44078794-44078966 | Common:1; Rare:47 | ||||
| chr17:44093439-44093587 | Common:1; Rare:59 | ||||
| chr17:44123594-44123840 | Common:3; Rare:72 | ||||
| chr17:44186637-44187045 | Common:1; Rare:143 | ||||
| chr17:44187161-44187274 | Rare:31 | ||||
| chr17:44198722-44198843 | Rare:41 | ||||
| chr17:44200107-44200225 | Common:1; Rare:59 | ||||
| chr17:44210884-44211229 | Common:1; Rare:105 | ||||
| chr17:44220810-44220965 | Rare:47 | ||||
| chr17:44221273-44221374 | Rare:31 | ||||
| chr17:44324737-44324976 | Common:3; Rare:91 | ||||
| chr17:44350439-44350798 | Rare:124; Clinvar:8; Clinvar (benign):5 | ||||
| chr17:44352008-44352571 | Common:1; Rare:185; Clinvar:17; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr17:44503370-44503714 | Rare:134 | ||||
| chr17:44557110-44557373 | Common:1; Rare:46 |