| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14643627-14643867 | Common:1; Rare:86 | ||||
| chr11:14892190-14892386 | Rare:62 | ||||
| chr11:16738456-16738854 | Common:3; Rare:93 | ||||
| chr11:17077608-17077893 | Common:2; Rare:121 | ||||
| chr11:17207856-17208102 | Common:2; Rare:88 | ||||
| chr11:17276475-17276823 | Common:5; Rare:102; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:18322075-18322312 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322514-18322616 | Common:2; Rare:49 | ||||
| chr11:18526835-18526957 | Rare:62 | ||||
| chr11:18588672-18588839 | Common:2; Rare:53 | ||||
| chr11:18698661-18698809 | Common:4; Rare:40 | ||||
| chr11:18791773-18791857 | Rare:29 | ||||
| chr11:20387417-20387720 | Common:7; Rare:96 | ||||
| chr11:22625515-22625622 | Rare:57; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625813-22626002 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):1 |