| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:129279478-129279738 | Common:3; Rare:109 | ||||
| chr11:129895531-129895685 | Common:2; Rare:60 | ||||
| chr11:130002205-130002366 | Rare:43 | ||||
| chr11:130002447-130002643 | Rare:42 | ||||
| chr11:130002820-130003013 | Common:1; Rare:37 | ||||
| chr11:130003015-130003322 | Common:1; Rare:124 | ||||
| chr11:130069603-130069944 | Common:2; Rare:128 | ||||
| chr11:130159665-130159834 | Common:1; Rare:50 | ||||
| chr11:130314862-130315091 | Common:2; Rare:82 | ||||
| chr11:130448406-130448550 | Rare:35 | ||||
| chr11:130916400-130916613 | Common:5; Rare:73 | ||||
| chr11:133956961-133957137 | Common:1; Rare:53 | ||||
| chr11:134223903-134224169 | Common:2; Rare:95 | ||||
| chr11:134224490-134224842 | Common:2; Rare:141 | ||||
| chr11:134253303-134253608 | Common:2; Rare:108; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |