| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20387343-20387810 | Common:25; Rare:389 | ||||
| chr11:22192867-22193153 | Rare:60 | ||||
| chr11:22624830-22625250 | Common:7; Rare:285; Clinvar:18; Clinvar (benign):19; Clinvar (pathogenic):2 | ||||
| chr11:22625162-22625314 | Common:2; Rare:57; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:22625443-22625653 | Common:1; Rare:241; Clinvar:13; Clinvar (benign):7; Clinvar (pathogenic):6 | ||||
| chr11:22625726-22626076 | Common:8; Rare:263; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr11:22829299-22829476 | Common:4; Rare:109 | ||||
| chr11:22829520-22829700 | Common:2; Rare:62 | ||||
| chr11:22829718-22830068 | Common:8; Rare:242 | ||||
| chr11:24496737-24496927 | Common:1; Rare:51 | ||||
| chr11:27362760-27363120 | Common:2; Rare:146 | ||||
| chr11:27363078-27363466 | Rare:255 | ||||
| chr11:27471748-27472237 | Common:12; Rare:284 | ||||
| chr11:27472679-27473062 | Common:9; Rare:158 | ||||
| chr11:27506700-27506994 | Common:3; Rare:244 |