| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:24722490-24723020 | Common:1; Rare:176 | ||||
| chr10:24723673-24724005 | Common:3; Rare:110 | ||||
| chr10:24952349-24953320 | Common:8; Rare:384 | ||||
| chr10:25016440-25016695 | Common:8; Rare:103 | ||||
| chr10:25016860-25017220 | Common:10; Rare:230 | ||||
| chr10:26697395-26697727 | Common:3; Rare:137; Clinvar (benign):2 | ||||
| chr10:26860554-26860709 | Common:1; Rare:32 | ||||
| chr10:26860834-26861310 | Common:11; Rare:235 | ||||
| chr10:27100394-27100622 | Common:7; Rare:117; Clinvar:8; Clinvar (benign):4 | ||||
| chr10:27154234-27154547 | Rare:147 | ||||
| chr10:27155161-27155412 | Common:12; Rare:192; Clinvar:10; Clinvar (benign):12 | ||||
| chr10:27240396-27240623 | Common:1; Rare:88 | ||||
| chr10:27240530-27241120 | Common:5; Rare:182 | ||||
| chr10:27242040-27242510 | Common:3; Rare:230 | ||||
| chr10:27504031-27504430 | Rare:310; Clinvar:9; Clinvar (benign):2 |