| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48553007-48553023 | Rare:4 | ||||
| chr17:50054917-50055270 | Common:2; Rare:66 | ||||
| chr17:50189852-50190115 | Common:1; Rare:76; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50197716-50197814 | Rare:24; Clinvar:3 | ||||
| chr17:50197818-50198023 | Common:4; Rare:67; Clinvar (benign):7 | ||||
| chr17:50286184-50286435 | Common:3; Rare:41 | ||||
| chr17:50302681-50302748 | Rare:15 | ||||
| chr17:50307652-50307961 | Rare:52 | ||||
| chr17:50317793-50317845 | Rare:5 | ||||
| chr17:50347031-50347037 | Rare:2 | ||||
| chr17:50347324-50347573 | Common:1; Rare:48 | ||||
| chr17:50351663-50351691 | Rare:3 | ||||
| chr17:50351729-50351965 | Common:1; Rare:39 | ||||
| chr17:50355220-50355534 | Common:2; Rare:64 | ||||
| chr17:50359672-50360224 | Common:2; Rare:106; Clinvar:2 |