| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17276010-17276400 | Common:8; Rare:243 | ||||
| chr11:17276404-17276827 | Common:28; Rare:596; Clinvar:22; Clinvar (pathogenic):7 | ||||
| chr11:17276764-17277507 | Common:9; Rare:251; Clinvar:1 | ||||
| chr11:17351280-17351810 | Common:4; Rare:162 | ||||
| chr11:17351750-17351893 | Common:1; Rare:25 | ||||
| chr11:17351830-17352060 | Common:2; Rare:80 | ||||
| chr11:17352241-17352641 | Common:2; Rare:91 | ||||
| chr11:17386603-17387003 | Common:5; Rare:128; Clinvar:8; Clinvar (benign):11 | ||||
| chr11:17389110-17389598 | Common:8; Rare:219 | ||||
| chr11:17544270-17544510 | Common:3; Rare:64; Clinvar:3 | ||||
| chr11:17544414-17544547 | Common:3; Rare:30 | ||||
| chr11:18011790-18012445 | Common:8; Rare:180 | ||||
| chr11:18012870-18013342 | Common:29; Rare:587 | ||||
| chr11:18105610-18105950 | Common:4; Rare:85 | ||||
| chr11:18105960-18106360 | Common:13; Rare:466 |