| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75205370-75205749 | Common:1; Rare:122 | ||||
| chr17:75261577-75261935 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr17:75271125-75271369 | Common:2; Rare:48 | ||||
| chr17:75289387-75289613 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75515426-75515782 | Common:3; Rare:102 | ||||
| chr17:75646100-75646354 | Common:4; Rare:55 | ||||
| chr17:75667127-75667465 | Common:5; Rare:114 | ||||
| chr17:75765123-75765293 | Common:1; Rare:52; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:75784564-75784872 | Common:2; Rare:136 | ||||
| chr17:75949215-75949546 | Common:1; Rare:90; Clinvar:3 | ||||
| chr17:75978945-75979298 | Rare:99; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:75979302-75979371 | Rare:13 | ||||
| chr17:75979374-75979490 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr17:76072498-76072691 | Rare:58 | ||||
| chr17:76103695-76103880 | Common:6; Rare:64 |