| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47323861-47323992 | Common:2; Rare:45 | ||||
| chr17:47831503-47831684 | Rare:53 | ||||
| chr17:47941356-47941708 | Rare:95; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47957829-47957997 | Rare:30 | ||||
| chr17:48048039-48048422 | Common:1; Rare:105 | ||||
| chr17:48101268-48101587 | Common:3; Rare:91 | ||||
| chr17:49210454-49210712 | Common:1; Rare:46 | ||||
| chr17:49414845-49415120 | Common:1; Rare:66 | ||||
| chr17:49677969-49678140 | Rare:46 | ||||
| chr17:49788564-49788724 | Common:1; Rare:50 | ||||
| chr17:50194608-50194805 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr17:50345911-50346159 | Common:4; Rare:84 | ||||
| chr17:50373168-50373235 | Common:2; Rare:28 | ||||
| chr17:50707611-50707849 | Common:4; Rare:76 | ||||
| chr17:50719444-50719661 | Common:1; Rare:86 |