| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75721135-75721677 | Common:11; Rare:397; Clinvar:8 | ||||
| chr17:75721582-75722279 | Common:1; Rare:151; Clinvar:1 | ||||
| chr17:75727280-75727940 | Common:2; Rare:329; Clinvar:5; Clinvar (pathogenic):5 | ||||
| chr17:75764576-75764785 | Common:1; Rare:58 | ||||
| chr17:75764760-75764866 | Rare:29 | ||||
| chr17:75765112-75765289 | Common:1; Rare:93; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr17:75779046-75779540 | Common:5; Rare:378 | ||||
| chr17:75779537-75780152 | Common:4; Rare:493 | ||||
| chr17:75784520-75785291 | Common:27; Rare:747 | ||||
| chr17:75844147-75844276 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:75844442-75844897 | Common:7; Rare:128; Clinvar:10; Clinvar (benign):4 | ||||
| chr17:75855231-75855778 | Common:6; Rare:400 | ||||
| chr17:75876000-75876201 | Rare:50 | ||||
| chr17:75876111-75876256 | Rare:31 | ||||
| chr17:75877100-75877580 | Common:4; Rare:95 |