| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47323890-47323995 | Common:1; Rare:31 | ||||
| chr17:47530977-47531279 | Rare:74 | ||||
| chr17:47649504-47649997 | Common:1; Rare:175 | ||||
| chr17:47896045-47896270 | Rare:66 | ||||
| chr17:47941356-47941732 | Rare:102; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048061-48048458 | Rare:111 | ||||
| chr17:48048653-48048864 | Common:3; Rare:35 | ||||
| chr17:48100981-48101082 | Rare:22 | ||||
| chr17:48107412-48107595 | Common:4; Rare:46 | ||||
| chr17:48107687-48107802 | Common:1; Rare:27 | ||||
| chr17:48544225-48544351 | Common:2; Rare:19 | ||||
| chr17:48544454-48544503 | Common:1; Rare:14 | ||||
| chr17:48544531-48544633 | Rare:40 | ||||
| chr17:48908300-48908407 | Common:1; Rare:25 | ||||
| chr17:48908606-48908751 | Rare:28 |