Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174999621-175000156 | Common:3; Rare:177 | ||||
chr1:178725131-178725316 | Common:10; Rare:71 | ||||
chr1:179882156-179882324 | Common:1; Rare:32 | ||||
chr1:179882478-179882879 | Rare:193; Clinvar:8; Clinvar (benign):2 | ||||
chr1:180502338-180502658 | Common:1; Rare:112 | ||||
chr1:181088494-181088719 | Rare:74 | ||||
chr1:182391331-182391480 | Rare:32 | ||||
chr1:182839247-182839399 | Common:1; Rare:67 | ||||
chr1:183472261-183472519 | Common:2; Rare:91 | ||||
chr1:183635666-183636114 | Common:5; Rare:126 | ||||
chr1:184051593-184051773 | Common:3; Rare:70 | ||||
chr1:185156929-185157277 | Common:1; Rare:93 | ||||
chr1:186375104-186375508 | Rare:113 | ||||
chr1:186375673-186375916 | Common:1; Rare:63 | ||||
chr1:193059330-193059671 | Rare:160 |