| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:32435525-32435629 | Common:1; Rare:14 | ||||
| chr11:32435631-32435832 | Rare:70 | ||||
| chr11:32435853-32436000 | Common:1; Rare:29 | ||||
| chr11:32583622-32583929 | Rare:109 | ||||
| chr11:32829833-32829957 | Common:3; Rare:33 | ||||
| chr11:33015762-33015935 | Common:2; Rare:68 | ||||
| chr11:33257157-33257439 | Common:3; Rare:98 | ||||
| chr11:33257511-33257737 | Common:1; Rare:52 | ||||
| chr11:33258130-33258617 | Common:2; Rare:177 | ||||
| chr11:33736390-33736606 | Common:2; Rare:67 | ||||
| chr11:33774473-33774614 | Common:2; Rare:51 | ||||
| chr11:34051595-34051732 | Rare:54 | ||||
| chr11:34052126-34052466 | Common:4; Rare:158 | ||||
| chr11:34105481-34105730 | Common:2; Rare:82 | ||||
| chr11:34438784-34439005 | Common:2; Rare:75; Clinvar (benign):1 |