Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155262120-155262506 | Common:3; Rare:121 | ||||
chr1:155273443-155273679 | Rare:81 | ||||
chr1:155308567-155308613 | Rare:8 | ||||
chr1:155308615-155309127 | Common:1; Rare:100 | ||||
chr1:155317712-155318029 | Common:1; Rare:55; Clinvar (pathogenic):1 | ||||
chr1:155318704-155318931 | Rare:60 | ||||
chr1:155319573-155319624 | Rare:17 | ||||
chr1:155320379-155320979 | Common:2; Rare:211 | ||||
chr1:155323155-155323509 | Rare:62 | ||||
chr1:155323812-155323966 | Rare:34 | ||||
chr1:155324160-155324614 | Common:3; Rare:162 | ||||
chr1:155349429-155349699 | Common:1; Rare:62 | ||||
chr1:155562218-155562423 | Rare:97 | ||||
chr1:155562727-155563005 | Common:1; Rare:148 | ||||
chr1:155563085-155563278 | Rare:83 |