Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155688591-155689136 | Common:2; Rare:168 | ||||
chr1:155857166-155857445 | Common:1; Rare:63 | ||||
chr1:155859330-155859686 | Common:3; Rare:74 | ||||
chr1:155934280-155934577 | Common:1; Rare:114 | ||||
chr1:155978150-155978247 | Rare:28 | ||||
chr1:155978478-155978633 | Rare:40 | ||||
chr1:155979097-155979240 | Common:1; Rare:23 | ||||
chr1:156053752-156053926 | Rare:45 | ||||
chr1:156054560-156054897 | Common:4; Rare:94 | ||||
chr1:156082442-156082578 | Rare:30 | ||||
chr1:156134800-156135285 | Common:3; Rare:115; Clinvar:22; Clinvar (benign):16; Clinvar (pathogenic):11 | ||||
chr1:156135899-156136438 | Common:4; Rare:174; Clinvar:39; Clinvar (benign):24; Clinvar (pathogenic):15 | ||||
chr1:156193832-156194145 | Common:3; Rare:79 | ||||
chr1:156212882-156213125 | Common:1; Rare:84 | ||||
chr1:156282751-156282954 | Common:3; Rare:67 |