| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45148152-45148620 | Common:1; Rare:160 | ||||
| chr17:45161536-45161911 | Common:1; Rare:90 | ||||
| chr17:45490713-45490867 | Rare:53 | ||||
| chr17:45894247-45894686 | Common:4; Rare:126; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:46922869-46923187 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189246-47189563 | Rare:80 | ||||
| chr17:47649614-47649965 | Common:1; Rare:134 | ||||
| chr17:47831503-47831670 | Rare:46 | ||||
| chr17:47896037-47896256 | Rare:58 | ||||
| chr17:47941368-47941732 | Rare:100; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970751-47971149 | Common:4; Rare:91 | ||||
| chr17:48048061-48048400 | Rare:90 | ||||
| chr17:48100989-48101601 | Common:3; Rare:165 | ||||
| chr17:48544216-48544340 | Common:1; Rare:16 | ||||
| chr17:48590239-48590428 | Common:1; Rare:42 |