Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:30016950-30017087 | Rare:35 | ||||
chr11:31369737-31369882 | Rare:45 | ||||
chr11:31509575-31509784 | Common:1; Rare:65 | ||||
chr11:32435875-32435971 | Rare:16 | ||||
chr11:33161449-33161678 | Common:6; Rare:63 | ||||
chr11:33257133-33257507 | Common:3; Rare:114 | ||||
chr11:33257592-33257743 | Rare:36 | ||||
chr11:33257814-33257882 | Rare:17 | ||||
chr11:33258130-33258371 | Rare:92 | ||||
chr11:33736391-33736586 | Common:2; Rare:63 | ||||
chr11:34052126-34052624 | Common:4; Rare:222 | ||||
chr11:34438755-34439016 | Common:2; Rare:86; Clinvar (benign):1 | ||||
chr11:34916287-34916657 | Common:10; Rare:149; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
chr11:36510229-36510377 | Rare:45 | ||||
chr11:43358814-43358983 | Rare:81 |