Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:91500796-91500909 | Common:2; Rare:43 | ||||
chr1:91886078-91886340 | Rare:110 | ||||
chr1:92298939-92299076 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92784627-92784862 | Common:1; Rare:64 | ||||
chr1:92784956-92785162 | Common:2; Rare:83 | ||||
chr1:92785165-92785368 | Common:5; Rare:48 | ||||
chr1:93079092-93079319 | Common:3; Rare:96 | ||||
chr1:93180291-93180751 | Common:2; Rare:183 | ||||
chr1:93345766-93345919 | Common:4; Rare:61 | ||||
chr1:93447996-93448238 | Common:2; Rare:79 | ||||
chr1:93879134-93879274 | Common:1; Rare:50 | ||||
chr1:94418216-94418489 | Common:2; Rare:97 | ||||
chr1:94541730-94542011 | Rare:79 | ||||
chr1:94820140-94820456 | Common:4; Rare:80 | ||||
chr1:94925739-94925930 | Rare:34 |