| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42288356-42288632 | Rare:46 | ||||
| chr17:42288821-42289198 | Common:5; Rare:76 | ||||
| chr17:42388345-42388949 | Common:1; Rare:159; Clinvar:3 | ||||
| chr17:42423233-42423365 | Common:1; Rare:36; Clinvar:1 | ||||
| chr17:42458669-42458991 | Common:3; Rare:119 | ||||
| chr17:42536041-42536306 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:42536521-42536815 | Common:3; Rare:72; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr17:42537024-42537218 | Common:2; Rare:31 | ||||
| chr17:42561948-42562228 | Common:1; Rare:80 | ||||
| chr17:42566922-42567296 | Common:4; Rare:126 | ||||
| chr17:42567429-42567557 | Common:1; Rare:32 | ||||
| chr17:42567562-42567641 | Rare:28 | ||||
| chr17:42567836-42567879 | Common:1; Rare:9 | ||||
| chr17:42577605-42578222 | Common:3; Rare:222 | ||||
| chr17:42578299-42578931 | Common:6; Rare:125 |