| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:46833060-46833221 | Common:2; Rare:27 | ||||
| chr17:46922831-46923203 | Common:9; Rare:210; Clinvar:4; Clinvar (benign):15 | ||||
| chr17:47189165-47189568 | Common:1; Rare:109 | ||||
| chr17:47323660-47324180 | Common:9; Rare:274 | ||||
| chr17:47530977-47531215 | Rare:102 | ||||
| chr17:47649414-47650088 | Common:3; Rare:437 | ||||
| chr17:47650448-47650817 | Common:6; Rare:261 | ||||
| chr17:47693983-47694096 | Rare:10 | ||||
| chr17:47694433-47694609 | Common:8; Rare:84 | ||||
| chr17:47821754-47821897 | Common:1; Rare:31 | ||||
| chr17:47831465-47831662 | Rare:111 | ||||
| chr17:47841081-47841384 | Rare:107 | ||||
| chr17:47895764-47896089 | Common:4; Rare:179 | ||||
| chr17:47896327-47896727 | Common:3; Rare:120 | ||||
| chr17:47941323-47941911 | Rare:264; Clinvar:15; Clinvar (benign):14; Clinvar (pathogenic):3 |