| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75904871-75905218 | Common:4; Rare:94 | ||||
| chr17:75949236-75949546 | Common:1; Rare:84; Clinvar:3 | ||||
| chr17:75979103-75979283 | Rare:50; Clinvar:4 | ||||
| chr17:76103712-76103867 | Common:4; Rare:49 | ||||
| chr17:76501385-76501572 | Rare:62; Clinvar (benign):3 | ||||
| chr17:76726462-76726872 | Common:5; Rare:153 | ||||
| chr17:76737309-76737438 | Common:3; Rare:60 | ||||
| chr17:78130686-78130810 | Rare:25 | ||||
| chr17:78168510-78168709 | Common:3; Rare:54 | ||||
| chr17:78187045-78187386 | Common:3; Rare:109 | ||||
| chr17:78782224-78782570 | Common:9; Rare:116 | ||||
| chr17:78840745-78841116 | Common:2; Rare:140 | ||||
| chr17:80035855-80036030 | Common:1; Rare:61 | ||||
| chr17:80220309-80220453 | Rare:57; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80384777-80385080 | Common:1; Rare:69 |