Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15847351-15848000 | Common:1; Rare:1446 | ||||
chr1:15847988-15848826 | Common:3; Rare:355 | ||||
chr1:15952422-15953120 | Common:6; Rare:261 | ||||
chr1:15953416-15953846 | Rare:145 | ||||
chr1:15975218-15975705 | Common:6; Rare:218 | ||||
chr1:15975990-15976390 | Common:8; Rare:243 | ||||
chr1:16017497-16017897 | Common:2; Rare:182 | ||||
chr1:16048390-16048941 | Common:21; Rare:384; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
chr1:16048850-16049110 | Common:4; Rare:163; Clinvar (benign):2 | ||||
chr1:16073230-16073900 | Common:18; Rare:310 | ||||
chr1:16073895-16074115 | Rare:45 | ||||
chr1:16145790-16146190 | Common:5; Rare:143 | ||||
chr1:16146105-16146357 | Common:6; Rare:56 | ||||
chr1:16146301-16146640 | Common:8; Rare:250 | ||||
chr1:16206380-16207369 | Common:50; Rare:1167 |