| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77127731-77127895 | Rare:29 | ||||
| chr17:77140630-77141059 | Common:3; Rare:149 | ||||
| chr17:77319454-77319602 | Common:3; Rare:37; Clinvar (benign):3 | ||||
| chr17:78186990-78187371 | Common:3; Rare:134 | ||||
| chr17:78379138-78379326 | Rare:39 | ||||
| chr17:78782240-78782575 | Common:9; Rare:112 | ||||
| chr17:78840745-78841104 | Common:2; Rare:135 | ||||
| chr17:80147109-80147371 | Common:5; Rare:104 | ||||
| chr17:80220309-80220469 | Common:1; Rare:62; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415115-80415212 | Common:1; Rare:69 | ||||
| chr17:81239036-81239317 | Common:2; Rare:92 | ||||
| chr17:81666268-81666364 | Rare:23 | ||||
| chr17:81666554-81666818 | Common:1; Rare:115 | ||||
| chr17:81683676-81684076 | Common:4; Rare:203 | ||||
| chr17:81703274-81703551 | Common:2; Rare:86; Clinvar (benign):2 |