Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:51990674-51990819 | Common:1; Rare:40 | ||||
chr1:52033340-52033495 | Common:8; Rare:113 | ||||
chr1:52033584-52033889 | Common:3; Rare:98 | ||||
chr1:52055146-52055391 | Common:3; Rare:61 | ||||
chr1:52055497-52055615 | Rare:18 | ||||
chr1:52056133-52056482 | Rare:92 | ||||
chr1:52141967-52142096 | Rare:25 | ||||
chr1:52142800-52142967 | Rare:40 | ||||
chr1:52366118-52366319 | Common:1; Rare:59 | ||||
chr1:52403730-52404070 | Common:1; Rare:65 | ||||
chr1:52404355-52404690 | Common:1; Rare:91 | ||||
chr1:52553032-52553153 | Common:1; Rare:46 | ||||
chr1:52553360-52553950 | Common:3; Rare:156 | ||||
chr1:52698065-52698199 | Common:1; Rare:31 | ||||
chr1:52698279-52698523 | Common:3; Rare:81; Clinvar (pathogenic):1 |