Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52056147-52056371 | Rare:64 | ||||
chr1:52141864-52142187 | Rare:88 | ||||
chr1:52404393-52404637 | Common:1; Rare:72 | ||||
chr1:52553020-52553375 | Common:4; Rare:105 | ||||
chr1:52698056-52698172 | Rare:26 | ||||
chr1:52698318-52698460 | Common:2; Rare:50 | ||||
chr1:52842681-52842881 | Common:1; Rare:78 | ||||
chr1:52911628-52911735 | Rare:38 | ||||
chr1:52927170-52927393 | Common:4; Rare:74 | ||||
chr1:53196649-53196884 | Rare:89; Clinvar:6; Clinvar (benign):1 | ||||
chr1:53220561-53220712 | Common:2; Rare:75 | ||||
chr1:53238460-53238699 | Common:2; Rare:89 | ||||
chr1:53946255-53946482 | Rare:81 | ||||
chr1:54053160-54053664 | Common:6; Rare:172 | ||||
chr1:54199993-54200252 | Rare:76 |