| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76501372-76501572 | Rare:67; Clinvar (benign):3 | ||||
| chr17:76726464-76726865 | Common:5; Rare:144 | ||||
| chr17:76737306-76737537 | Common:3; Rare:94 | ||||
| chr17:76737852-76738079 | Common:3; Rare:63 | ||||
| chr17:78187052-78187376 | Common:3; Rare:102 | ||||
| chr17:78378581-78378692 | Common:1; Rare:51 | ||||
| chr17:78782255-78782555 | Common:9; Rare:95 | ||||
| chr17:78840774-78840993 | Common:2; Rare:81 | ||||
| chr17:80220310-80220453 | Rare:57; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415105-80415189 | Common:1; Rare:56 | ||||
| chr17:81636922-81637246 | Common:3; Rare:128 | ||||
| chr17:81666565-81666758 | Common:1; Rare:82 | ||||
| chr17:81683670-81684057 | Common:4; Rare:198 | ||||
| chr17:81703267-81703475 | Common:2; Rare:61; Clinvar (benign):2 | ||||
| chr17:81891404-81891821 | Common:3; Rare:167 |