| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45316957-45317346 | Common:5; Rare:97 | ||||
| chr17:45490752-45490921 | Common:6; Rare:52 | ||||
| chr17:46032246-46032510 | Common:2; Rare:50; Clinvar (benign):1 | ||||
| chr17:46045631-46045677 | Rare:11 | ||||
| chr17:46923051-46923198 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):7 | ||||
| chr17:47189181-47189595 | Common:1; Rare:112 | ||||
| chr17:47323864-47324025 | Common:1; Rare:60 | ||||
| chr17:47649416-47650074 | Common:2; Rare:228 | ||||
| chr17:47650115-47650438 | Rare:112 | ||||
| chr17:47694434-47694555 | Common:3; Rare:36 | ||||
| chr17:47831448-47831724 | Rare:89 | ||||
| chr17:47895745-47895874 | Common:3; Rare:30 | ||||
| chr17:47895896-47896286 | Rare:124 | ||||
| chr17:47941337-47941777 | Rare:117; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:48048032-48048462 | Common:1; Rare:120 |