| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42423014-42423454 | Common:1; Rare:129; Clinvar:3 | ||||
| chr17:42458730-42458936 | Common:3; Rare:76 | ||||
| chr17:42566988-42567155 | Common:3; Rare:54 | ||||
| chr17:42577658-42577805 | Rare:68 | ||||
| chr17:42609327-42609732 | Common:8; Rare:171; Clinvar (benign):2 | ||||
| chr17:42761075-42761263 | Rare:52 | ||||
| chr17:42773369-42773495 | Rare:38 | ||||
| chr17:42780519-42780642 | Common:1; Rare:43 | ||||
| chr17:42833351-42833491 | Rare:54 | ||||
| chr17:42964428-42964579 | Common:1; Rare:62 | ||||
| chr17:43006744-43006823 | Rare:19 | ||||
| chr17:43125354-43125590 | Rare:40; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170982-43171274 | Common:1; Rare:99 | ||||
| chr17:44070619-44070963 | Common:3; Rare:121; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44186620-44187002 | Common:1; Rare:138 |