| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58331217-58331570 | Rare:86 | ||||
| chr17:58331571-58331590 | Rare:3 | ||||
| chr17:58332468-58332815 | Common:3; Rare:85 | ||||
| chr17:58336931-58337520 | Common:2; Rare:69 | ||||
| chr17:58338142-58338317 | Common:1; Rare:43 | ||||
| chr17:58339049-58339222 | Rare:30 | ||||
| chr17:58346267-58346556 | Common:1; Rare:57 | ||||
| chr17:58518659-58518801 | Rare:26 | ||||
| chr17:58631796-58632140 | Common:8; Rare:166 | ||||
| chr17:59673549-59673769 | Common:1; Rare:47; Clinvar (pathogenic):1 | ||||
| chr17:59676729-59677051 | Rare:64 | ||||
| chr17:59839342-59839588 | Rare:41 | ||||
| chr17:60089190-60089288 | Rare:14 | ||||
| chr17:60134898-60135039 | Rare:20 | ||||
| chr17:61135983-61136201 | Common:1; Rare:42 |