Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149886637-149886987 | Common:2; Rare:133 | ||||
chr1:149887328-149887636 | Rare:200 | ||||
chr1:149887910-149888221 | Rare:93 | ||||
chr1:149927263-149927361 | Rare:29 | ||||
chr1:149927727-149927901 | Common:1; Rare:66; Clinvar (benign):5 | ||||
chr1:149931485-149931828 | Common:3; Rare:50 | ||||
chr1:150010588-150010867 | Common:2; Rare:70 | ||||
chr1:150067114-150067384 | Common:4; Rare:54 | ||||
chr1:150067646-150067950 | Rare:93 | ||||
chr1:150149481-150149667 | Rare:40 | ||||
chr1:150149689-150150287 | Common:5; Rare:215 | ||||
chr1:150235734-150236224 | Common:3; Rare:100 | ||||
chr1:150267697-150267966 | Common:2; Rare:63 | ||||
chr1:150268427-150268574 | Rare:33 | ||||
chr1:150269596-150269941 | Common:3; Rare:60 |