Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:53970774-53971152 | Common:11; Rare:138 | ||||
chr2:54115892-54115970 | Common:1; Rare:33 | ||||
chr2:54330763-54330919 | Common:3; Rare:57 | ||||
chr2:54456068-54456427 | Common:2; Rare:140 | ||||
chr2:54558649-54558781 | Common:1; Rare:35 | ||||
chr2:55010217-55010366 | Rare:34 | ||||
chr2:55050441-55050763 | Common:4; Rare:96 | ||||
chr2:55232245-55232415 | Common:3; Rare:41 | ||||
chr2:55519394-55519913 | Common:2; Rare:169 | ||||
chr2:55923725-55923856 | Common:2; Rare:42; Clinvar (benign):4 | ||||
chr2:55924101-55924340 | Common:4; Rare:39; Clinvar:1; Clinvar (benign):2 | ||||
chr2:58046612-58046845 | Rare:71 | ||||
chr2:58047220-58047289 | Rare:23 | ||||
chr2:60756149-60756312 | Rare:58 | ||||
chr2:60881315-60881773 | Common:3; Rare:154 |