Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179877713-179877844 | Rare:34 | ||||
chr1:179882038-179882306 | Common:2; Rare:62 | ||||
chr1:179882482-179882966 | Common:1; Rare:244; Clinvar:11; Clinvar (benign):4 | ||||
chr1:179954697-179954822 | Rare:28 | ||||
chr1:180154495-180154923 | Common:3; Rare:140 | ||||
chr1:180502173-180502641 | Common:1; Rare:171 | ||||
chr1:180502824-180503137 | Rare:106 | ||||
chr1:181088857-181089300 | Common:4; Rare:163 | ||||
chr1:182391331-182391452 | Rare:25 | ||||
chr1:182391678-182391714 | Common:1; Rare:9; Clinvar (benign):1 | ||||
chr1:182789615-182789786 | Common:2; Rare:56 | ||||
chr1:182839076-182839679 | Common:4; Rare:212 | ||||
chr1:182858565-182858888 | Common:2; Rare:67 | ||||
chr1:183023044-183023385 | Common:5; Rare:86 | ||||
chr1:183134655-183135180 | Common:3; Rare:122 |