Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179954697-179954814 | Rare:28 | ||||
chr1:180154615-180154932 | Common:4; Rare:102 | ||||
chr1:180155028-180155169 | Common:1; Rare:37 | ||||
chr1:180502253-180502715 | Common:1; Rare:166 | ||||
chr1:181088519-181088823 | Common:1; Rare:117 | ||||
chr1:181088857-181089033 | Common:1; Rare:68 | ||||
chr1:182391308-182391494 | Rare:40 | ||||
chr1:182391708-182392021 | Common:3; Rare:116; Clinvar:5; Clinvar (benign):3 | ||||
chr1:182789693-182789790 | Common:1; Rare:36 | ||||
chr1:182839205-182839453 | Common:1; Rare:98 | ||||
chr1:182839559-182839725 | Common:2; Rare:76 | ||||
chr1:182858556-182858888 | Common:2; Rare:69 | ||||
chr1:183134634-183135180 | Common:3; Rare:130 | ||||
chr1:183186121-183186278 | Common:2; Rare:23; Clinvar (benign):2 | ||||
chr1:183472254-183472526 | Common:2; Rare:94 |