| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8162917-8163071 | Rare:49 | ||||
| chr17:8248032-8248119 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249024-8249317 | Common:1; Rare:63 | ||||
| chr17:8435679-8436039 | Common:4; Rare:139 | ||||
| chr17:8965667-8965911 | Common:2; Rare:67 | ||||
| chr17:9645417-9645728 | Common:1; Rare:71 | ||||
| chr17:9645855-9645968 | Rare:20 | ||||
| chr17:10697472-10697654 | Common:3; Rare:85; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:10729749-10729843 | Rare:50 | ||||
| chr17:10729955-10730177 | Common:3; Rare:46 | ||||
| chr17:11997413-11997602 | Rare:68 | ||||
| chr17:13017626-13017696 | Rare:30 | ||||
| chr17:14069347-14069648 | Common:3; Rare:114; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:14300806-14301103 | Common:2; Rare:81 | ||||
| chr17:15262460-15262735 | Rare:59 |