Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173824331-173824708 | Rare:75; Clinvar:1 | ||||
chr1:173867975-173868054 | Rare:31 | ||||
chr1:174999292-174999423 | Common:1; Rare:40 | ||||
chr1:174999612-175000114 | Common:1; Rare:154 | ||||
chr1:175023404-175023626 | Common:1; Rare:60 | ||||
chr1:178341320-178341539 | Common:1; Rare:43 | ||||
chr1:178724937-178725309 | Common:12; Rare:128 | ||||
chr1:179143045-179143205 | Rare:30 | ||||
chr1:179293672-179293855 | Common:2; Rare:63 | ||||
chr1:179877756-179877856 | Rare:25 | ||||
chr1:179882220-179882308 | Rare:16 | ||||
chr1:179882481-179882874 | Rare:188; Clinvar:8; Clinvar (benign):2 | ||||
chr1:180502513-180502678 | Common:1; Rare:69 | ||||
chr1:181088493-181088704 | Rare:67 | ||||
chr1:182604385-182604565 | Rare:40 |