Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1233915-1234364 | Common:5; Rare:112 | ||||
chr1:1871938-1871958 | Common:1; Rare:4 | ||||
chr1:3631531-3631913 | Common:8; Rare:115 | ||||
chr1:9182105-9182240 | Rare:37 | ||||
chr1:9182368-9182497 | Common:2; Rare:32 | ||||
chr1:9428929-9429135 | Common:2; Rare:63 | ||||
chr1:9687507-9687634 | Common:1; Rare:34 | ||||
chr1:11070898-11071076 | Common:1; Rare:52 | ||||
chr1:11974379-11974833 | Common:2; Rare:118; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:12619012-12619204 | Rare:35 | ||||
chr1:15654695-15654886 | Rare:34 | ||||
chr1:15800239-15800343 | Rare:18 | ||||
chr1:15940364-15940538 | Common:1; Rare:39 | ||||
chr1:16499214-16499423 | Common:1; Rare:96 | ||||
chr1:16618400-16618764 | Common:8; Rare:7 |