| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7014543-7014794 | Common:4; Rare:89 | ||||
| chr17:7014872-7015101 | Common:2; Rare:75 | ||||
| chr17:7035759-7036055 | Common:1; Rare:70 | ||||
| chr17:7115890-7116270 | Common:3; Rare:90 | ||||
| chr17:7176845-7177030 | Common:2; Rare:63 | ||||
| chr17:7177487-7177712 | Common:1; Rare:60 | ||||
| chr17:7178110-7178281 | Rare:35 | ||||
| chr17:7204879-7205094 | Rare:47 | ||||
| chr17:7213910-7214175 | Common:1; Rare:52 | ||||
| chr17:7217604-7217737 | Common:1; Rare:23 | ||||
| chr17:7219725-7219975 | Common:3; Rare:101; Clinvar:6; Clinvar (benign):2 | ||||
| chr17:7220241-7220641 | Common:2; Rare:164; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr17:7234484-7234683 | Common:2; Rare:99 | ||||
| chr17:7237790-7237974 | Common:1; Rare:56 | ||||
| chr17:7239364-7239594 | Common:2; Rare:70 |