| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:73193605-73193673 | Rare:11 | ||||
| chr17:73645190-73645330 | Common:1; Rare:43 | ||||
| chr17:74794960-74795016 | Rare:15 | ||||
| chr17:75220903-75221043 | Common:3; Rare:23 | ||||
| chr17:75685003-75685307 | Common:2; Rare:47 | ||||
| chr17:75688319-75688422 | Rare:17 | ||||
| chr17:75723235-75723570 | Common:1; Rare:62 | ||||
| chr17:75729931-75730257 | Common:1; Rare:58 | ||||
| chr17:75736051-75736540 | Common:3; Rare:135; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr17:75736874-75737186 | Common:1; Rare:60 | ||||
| chr17:75739584-75739757 | Common:1; Rare:55 | ||||
| chr17:75740788-75741031 | Rare:84; Clinvar:1 | ||||
| chr17:75741145-75741411 | Common:2; Rare:41 | ||||
| chr17:75746105-75746241 | Rare:23 | ||||
| chr17:75747724-75747931 | Common:1; Rare:29 |