Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:171741918-171742160 | Common:1; Rare:79 | ||||
chr1:171781353-171781709 | Common:3; Rare:90 | ||||
chr1:173476978-173477442 | Common:5; Rare:158 | ||||
chr1:173824337-173824716 | Rare:75; Clinvar:2 | ||||
chr1:173867975-173868167 | Rare:71 | ||||
chr1:174022370-174022516 | Rare:42 | ||||
chr1:174999283-174999483 | Common:2; Rare:58 | ||||
chr1:174999599-175000119 | Common:1; Rare:162 | ||||
chr1:175023406-175023626 | Common:1; Rare:59 | ||||
chr1:177984276-177984415 | Rare:25 | ||||
chr1:178725114-178725309 | Common:10; Rare:76 | ||||
chr1:179293672-179293849 | Common:2; Rare:62 | ||||
chr1:179877771-179877930 | Rare:29 | ||||
chr1:179882478-179882816 | Rare:159; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179954512-179954811 | Common:1; Rare:72 |