| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:32829755-32829992 | Common:3; Rare:51 | ||||
| chr11:33039951-33040048 | Rare:31 | ||||
| chr11:33161384-33161657 | Common:7; Rare:68 | ||||
| chr11:33257039-33257479 | Common:3; Rare:134 | ||||
| chr11:33257560-33257754 | Rare:45 | ||||
| chr11:33257758-33257876 | Common:1; Rare:29 | ||||
| chr11:33258158-33258626 | Common:2; Rare:171 | ||||
| chr11:33700967-33701077 | Common:2; Rare:30 | ||||
| chr11:33774393-33774570 | Common:2; Rare:61 | ||||
| chr11:34051631-34051741 | Rare:51 | ||||
| chr11:34052159-34052624 | Common:4; Rare:210 | ||||
| chr11:34105481-34105778 | Common:2; Rare:95 | ||||
| chr11:34438787-34439049 | Common:2; Rare:87; Clinvar (benign):1 | ||||
| chr11:34620845-34621183 | Common:3; Rare:71 | ||||
| chr11:34624186-34624346 | Common:2; Rare:40 |