Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:778591-778820 | Common:5; Rare:98 | ||||
chr1:827461-827833 | Common:3; Rare:121 | ||||
chr1:904703-904897 | Common:1; Rare:60 | ||||
chr1:905502-905677 | Common:1; Rare:27 | ||||
chr1:1233123-1233373 | Rare:89; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:1746661-1746815 | Common:1; Rare:14 | ||||
chr1:4571375-4571516 | Rare:30 | ||||
chr1:6003846-6004094 | Common:2; Rare:58 | ||||
chr1:6090463-6090611 | Common:1; Rare:53 | ||||
chr1:6261763-6261885 | Rare:33 | ||||
chr1:7702431-7702572 | Common:1; Rare:36 | ||||
chr1:7704550-7704867 | Common:4; Rare:136 | ||||
chr1:8679488-8679563 | Rare:12 | ||||
chr1:8712436-8712450 | Rare:3 | ||||
chr1:9428848-9429135 | Common:2; Rare:91 |