| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42276658-42276735 | Rare:16 | ||||
| chr17:42387746-42387942 | Common:2; Rare:38 | ||||
| chr17:42388375-42388963 | Common:2; Rare:154; Clinvar:3 | ||||
| chr17:42423191-42423489 | Common:1; Rare:78; Clinvar:1 | ||||
| chr17:42458674-42458957 | Common:3; Rare:105 | ||||
| chr17:42536124-42536338 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:42536552-42536749 | Common:2; Rare:55; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr17:42536776-42536793 | Common:1; Rare:4 | ||||
| chr17:42548698-42548875 | Common:2; Rare:31 | ||||
| chr17:42561965-42562229 | Common:1; Rare:78 | ||||
| chr17:42566879-42567277 | Common:4; Rare:130 | ||||
| chr17:42577631-42577881 | Common:1; Rare:125 | ||||
| chr17:42609321-42609772 | Common:8; Rare:186; Clinvar (benign):2 | ||||
| chr17:42659144-42659399 | Rare:76 | ||||
| chr17:42676501-42676514 | Rare:2 |