Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23530786-23530886 | Common:1; Rare:24 | ||||
chr1:23531158-23531569 | Common:15; Rare:286 | ||||
chr1:23558159-23558710 | Common:7; Rare:338 | ||||
chr1:23558970-23559698 | Common:17; Rare:951 | ||||
chr1:23691450-23691910 | Common:17; Rare:344; Clinvar:8; Clinvar (benign):8 | ||||
chr1:23691905-23692486 | Common:3; Rare:320 | ||||
chr1:23742592-23742852 | Rare:42 | ||||
chr1:23742953-23743155 | Common:1; Rare:45 | ||||
chr1:23743120-23743550 | Common:1; Rare:452 | ||||
chr1:23743570-23743770 | Common:1; Rare:47 | ||||
chr1:23743853-23744087 | Rare:94 | ||||
chr1:23744508-23744908 | Common:6; Rare:74 | ||||
chr1:23777810-23778170 | Common:3; Rare:268 | ||||
chr1:23778143-23778647 | Common:61; Rare:926 | ||||
chr1:23778934-23779869 | Common:5; Rare:634 |