Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:148522297-148522680 | Common:7; Rare:150 | ||||
chr1:150160677-150160739 | Rare:19 | ||||
chr1:150611534-150611800 | Common:1; Rare:38 | ||||
chr1:151054841-151055116 | Common:1; Rare:62 | ||||
chr1:151056280-151056464 | Common:2; Rare:30 | ||||
chr1:151945736-151946050 | Common:3; Rare:61 | ||||
chr1:153665492-153665523 | Rare:6 | ||||
chr1:155227531-155227721 | Common:1; Rare:50 | ||||
chr1:155904481-155904738 | Common:2; Rare:77; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:155965080-155965336 | Common:1; Rare:45 | ||||
chr1:156097071-156097359 | Common:1; Rare:72 | ||||
chr1:156317219-156317518 | Rare:75 | ||||
chr1:156457298-156457623 | Common:2; Rare:65 | ||||
chr1:156505311-156505536 | Common:2; Rare:73 | ||||
chr1:157680729-157681040 | Common:3; Rare:85 |