| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39461193-39461612 | Common:7; Rare:414 | ||||
| chr17:39461674-39462974 | Common:18; Rare:1109 | ||||
| chr17:39636855-39637620 | Common:34; Rare:903 | ||||
| chr17:39663830-39664410 | Common:7; Rare:310 | ||||
| chr17:39667302-39668860 | Common:26; Rare:1417 | ||||
| chr17:39686946-39687681 | Common:6; Rare:144 | ||||
| chr17:39687625-39688025 | Rare:363; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr17:39688009-39688270 | Rare:302 | ||||
| chr17:39730159-39730901 | Common:9; Rare:600 | ||||
| chr17:39737688-39738088 | Rare:96 | ||||
| chr17:39738495-39738895 | Rare:95 | ||||
| chr17:39739180-39739580 | Common:1; Rare:74 | ||||
| chr17:39740422-39740878 | Common:5; Rare:187 | ||||
| chr17:39863790-39864491 | Common:14; Rare:545 | ||||
| chr17:39926740-39927120 | Common:1; Rare:106 |