Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:163321772-163322007 | Common:1; Rare:62 | ||||
chr1:165768814-165769055 | Common:2; Rare:103 | ||||
chr1:167935988-167936241 | Common:1; Rare:75 | ||||
chr1:168178724-168179015 | Common:4; Rare:84 | ||||
chr1:168225714-168226037 | Common:3; Rare:107 | ||||
chr1:169367944-169368254 | Common:1; Rare:60 | ||||
chr1:169794895-169795094 | Common:3; Rare:51 | ||||
chr1:173477144-173477484 | Common:4; Rare:124 | ||||
chr1:173824390-173824708 | Rare:57; Clinvar:1 | ||||
chr1:173867975-173868213 | Common:1; Rare:82 | ||||
chr1:174999621-175000114 | Common:1; Rare:148 | ||||
chr1:179882725-179882848 | Rare:56; Clinvar:5 | ||||
chr1:183186170-183186281 | Common:1; Rare:16; Clinvar (benign):1 | ||||
chr1:183635676-183635831 | Common:1; Rare:49 | ||||
chr1:186375686-186375911 | Common:1; Rare:59 |