| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63827556-63827797 | Common:1; Rare:55 | ||||
| chr17:63841842-63842009 | Rare:29 | ||||
| chr17:63842380-63842473 | Common:1; Rare:20 | ||||
| chr17:63842552-63843379 | Common:3; Rare:188 | ||||
| chr17:64129778-64130433 | Common:8; Rare:161 | ||||
| chr17:64130720-64130902 | Rare:32 | ||||
| chr17:64230836-64231134 | Common:1; Rare:43 | ||||
| chr17:64263057-64263505 | Common:3; Rare:139 | ||||
| chr17:64448924-64449224 | Common:3; Rare:37 | ||||
| chr17:64496348-64496629 | Common:1; Rare:100; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:64496782-64497300 | Common:5; Rare:219; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:64497509-64497535 | Rare:9 | ||||
| chr17:64504323-64504662 | Common:3; Rare:118 | ||||
| chr17:64505368-64505480 | Common:2; Rare:46 | ||||
| chr17:64505495-64505673 | Common:1; Rare:55 |