| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33161443-33161624 | Common:5; Rare:48 | ||||
| chr11:33257298-33257479 | Common:2; Rare:56 | ||||
| chr11:33257591-33257732 | Rare:35 | ||||
| chr11:33257814-33257889 | Rare:18 | ||||
| chr11:33258111-33258346 | Rare:91 | ||||
| chr11:33258465-33258626 | Rare:57 | ||||
| chr11:34052119-34052493 | Common:4; Rare:171 | ||||
| chr11:34105481-34105724 | Common:2; Rare:80 | ||||
| chr11:34357980-34358285 | Common:2; Rare:87 | ||||
| chr11:34438769-34439057 | Common:2; Rare:96; Clinvar (benign):1 | ||||
| chr11:34620906-34621161 | Common:2; Rare:50 | ||||
| chr11:34624224-34624311 | Common:2; Rare:20 | ||||
| chr11:34642667-34642824 | Common:2; Rare:45 | ||||
| chr11:34916102-34916657 | Common:13; Rare:211; Clinvar:6; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr11:35138949-35139332 | Common:1; Rare:103 |