| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44807865-44807939 | Rare:12 | ||||
| chr17:44829591-44829726 | Common:1; Rare:40 | ||||
| chr17:44829876-44830105 | Common:2; Rare:59 | ||||
| chr17:44899029-44899166 | Rare:37 | ||||
| chr17:44899346-44899833 | Common:4; Rare:136; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:44947473-44948000 | Common:2; Rare:137 | ||||
| chr17:45051289-45051328 | Rare:10 | ||||
| chr17:45051366-45051550 | Common:1; Rare:53 | ||||
| chr17:45052055-45052206 | Common:2; Rare:24 | ||||
| chr17:45060749-45060785 | Rare:2 | ||||
| chr17:45060793-45061431 | Common:3; Rare:171 | ||||
| chr17:45061500-45061713 | Rare:45 | ||||
| chr17:45132488-45132717 | Common:3; Rare:76 | ||||
| chr17:45135419-45135738 | Common:2; Rare:62 | ||||
| chr17:45148112-45148675 | Common:1; Rare:186 |