Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179081889-179082114 | Common:1; Rare:70 | ||||
chr1:179882208-179882308 | Rare:19 | ||||
chr1:179882516-179882852 | Rare:161; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179954647-179954827 | Common:1; Rare:39 | ||||
chr1:180502513-180502647 | Common:1; Rare:57 | ||||
chr1:181088570-181088704 | Rare:44 | ||||
chr1:182390842-182391010 | Rare:31 | ||||
chr1:182391286-182391454 | Rare:34 | ||||
chr1:182391744-182392016 | Common:3; Rare:92; Clinvar:4; Clinvar (benign):3 | ||||
chr1:182789615-182789792 | Common:2; Rare:61 | ||||
chr1:182839302-182839403 | Rare:51 | ||||
chr1:183023043-183023256 | Common:5; Rare:59 | ||||
chr1:183635634-183636047 | Common:2; Rare:113 | ||||
chr1:184051675-184051753 | Common:2; Rare:27 | ||||
chr1:184386907-184387368 | Common:1; Rare:103 |