| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:207340-207719 | Common:8; Rare:129 | ||||
| chr11:236837-237032 | Common:2; Rare:67 | ||||
| chr11:777471-777598 | Rare:55 | ||||
| chr11:809755-810023 | Common:1; Rare:119 | ||||
| chr11:842497-842886 | Common:7; Rare:160 | ||||
| chr11:1871236-1871416 | Common:3; Rare:46 | ||||
| chr11:5624893-5625005 | Rare:15 | ||||
| chr11:6390316-6390469 | Common:1; Rare:44 | ||||
| chr11:6481292-6481511 | Common:3; Rare:86 | ||||
| chr11:6603561-6603806 | Common:3; Rare:74 | ||||
| chr11:8682706-8682816 | Common:1; Rare:53 | ||||
| chr11:9663893-9664139 | Common:3; Rare:72 | ||||
| chr11:10858013-10858231 | Common:3; Rare:64 | ||||
| chr11:16738466-16738681 | Common:2; Rare:41 | ||||
| chr11:18322128-18322296 | Common:3; Rare:58; Clinvar:1; Clinvar (benign):2 |