| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63827597-63827800 | Common:1; Rare:38 | ||||
| chr17:63827827-63828169 | Common:2; Rare:148 | ||||
| chr17:63831365-63831876 | Common:3; Rare:240 | ||||
| chr17:63838606-63839105 | Common:6; Rare:215 | ||||
| chr17:63841399-63842158 | Common:3; Rare:156 | ||||
| chr17:63842410-63843280 | Common:10; Rare:413 | ||||
| chr17:64129962-64130395 | Common:19; Rare:305 | ||||
| chr17:64263172-64263566 | Common:7; Rare:326 | ||||
| chr17:64495942-64496930 | Common:6; Rare:451; Clinvar:15; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
| chr17:64496954-64497290 | Common:7; Rare:324; Clinvar:9; Clinvar (benign):8 | ||||
| chr17:64497492-64497597 | Common:1; Rare:46 | ||||
| chr17:64505348-64505658 | Common:7; Rare:244 | ||||
| chr17:64505668-64506068 | Common:19; Rare:241 | ||||
| chr17:64506059-64506550 | Common:14; Rare:539 | ||||
| chr17:64506572-64507123 | Common:12; Rare:490 |