| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39401486-39401820 | Common:1; Rare:85 | ||||
| chr17:39451244-39451403 | Common:2; Rare:57 | ||||
| chr17:39461868-39462104 | Common:3; Rare:66 | ||||
| chr17:39636978-39637193 | Common:4; Rare:74 | ||||
| chr17:39688020-39688189 | Rare:54 | ||||
| chr17:39864161-39864385 | Common:2; Rare:47 | ||||
| chr17:39927551-39927754 | Common:1; Rare:62 | ||||
| chr17:39980730-39980889 | Common:1; Rare:45 | ||||
| chr17:40140185-40140544 | Common:5; Rare:178 | ||||
| chr17:40219168-40219381 | Common:1; Rare:67 | ||||
| chr17:40318085-40318293 | Common:1; Rare:46 | ||||
| chr17:41688613-41688904 | Common:1; Rare:99 | ||||
| chr17:41689230-41689569 | Common:4; Rare:128 | ||||
| chr17:41771850-41771961 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr17:41930527-41930645 | Rare:28 |