| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45060975-45061341 | Common:2; Rare:98 | ||||
| chr17:45148147-45148608 | Common:1; Rare:156 | ||||
| chr17:45490713-45490880 | Rare:55 | ||||
| chr17:45620245-45620364 | Rare:30 | ||||
| chr17:46922869-46923187 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47323788-47324009 | Common:3; Rare:80 | ||||
| chr17:47831490-47831649 | Rare:47 | ||||
| chr17:47896210-47896281 | Rare:26 | ||||
| chr17:47941368-47941732 | Rare:100; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970843-47971170 | Common:1; Rare:79 | ||||
| chr17:48048069-48048400 | Rare:84 | ||||
| chr17:48048653-48048813 | Common:3; Rare:23 | ||||
| chr17:48107427-48107825 | Common:5; Rare:97 | ||||
| chr17:48544449-48544498 | Common:1; Rare:16 | ||||
| chr17:48544690-48544775 | Common:2; Rare:27 |