| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:46193411-46193610 | Common:3; Rare:54 | ||||
| chr17:46225353-46225476 | Common:1; Rare:32 | ||||
| chr17:46922827-46923187 | Common:4; Rare:99; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189235-47189563 | Rare:82 | ||||
| chr17:47323899-47323987 | Common:1; Rare:22 | ||||
| chr17:47821752-47821883 | Common:1; Rare:32 | ||||
| chr17:47831503-47831614 | Rare:33 | ||||
| chr17:47941356-47941713 | Rare:98; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048069-48048405 | Rare:86 | ||||
| chr17:48048602-48048813 | Common:4; Rare:30 | ||||
| chr17:48101111-48101528 | Common:3; Rare:108 | ||||
| chr17:48107664-48107768 | Common:1; Rare:22 | ||||
| chr17:48544562-48544619 | Rare:23 | ||||
| chr17:48590176-48590435 | Common:1; Rare:54 | ||||
| chr17:48604977-48605130 | Rare:28 |