| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3535475-3535875 | Rare:181 | ||||
| chr17:3557740-3558120 | Common:4; Rare:89; Clinvar:6; Clinvar (benign):5 | ||||
| chr17:3636169-3636569 | Common:31; Rare:671; Clinvar:1; Clinvar (benign):9 | ||||
| chr17:3636677-3636789 | Common:2; Rare:55; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:3639928-3640328 | Common:3; Rare:161; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:3667880-3668210 | Rare:74 | ||||
| chr17:3668387-3668890 | Common:15; Rare:890 | ||||
| chr17:3695910-3696470 | Common:3; Rare:256 | ||||
| chr17:3723674-3724125 | Common:6; Rare:891 | ||||
| chr17:3724130-3724530 | Common:4; Rare:150 | ||||
| chr17:3754590-3755229 | Common:34; Rare:373 | ||||
| chr17:3846133-3846573 | Common:4; Rare:321 | ||||
| chr17:3892900-3893313 | Common:17; Rare:671 | ||||
| chr17:3916030-3916854 | Common:7; Rare:491 | ||||
| chr17:3916936-3917354 | Common:5; Rare:167 |