| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44947702-44947936 | Common:1; Rare:71 | ||||
| chr17:45060950-45061339 | Common:3; Rare:99 | ||||
| chr17:45148160-45148476 | Common:1; Rare:91 | ||||
| chr17:46193424-46193600 | Common:3; Rare:51 | ||||
| chr17:46923048-46923187 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189242-47189591 | Rare:89 | ||||
| chr17:47649534-47649816 | Common:1; Rare:82 | ||||
| chr17:47694493-47694605 | Common:3; Rare:27 | ||||
| chr17:47941356-47941707 | Rare:95; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048039-48048405 | Common:1; Rare:100 | ||||
| chr17:48054389-48054715 | Rare:56 | ||||
| chr17:48101280-48101587 | Common:3; Rare:89 | ||||
| chr17:48107427-48107599 | Common:3; Rare:41 | ||||
| chr17:48817032-48817331 | Common:1; Rare:70 | ||||
| chr17:48944758-48944920 | Common:2; Rare:57 |