Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:61951296-61951586 | Rare:60 | ||||
chr1:62495580-62495760 | Rare:23; Clinvar:1 | ||||
chr1:62517114-62517314 | Common:1; Rare:37 | ||||
chr1:62688252-62688533 | Common:1; Rare:109; Clinvar:1 | ||||
chr1:62784056-62784181 | Rare:47 | ||||
chr1:63523155-63523612 | Common:3; Rare:127 | ||||
chr1:63592974-63593499 | Rare:146; Clinvar (benign):1 | ||||
chr1:63593637-63593715 | Rare:41; Clinvar (pathogenic):1 | ||||
chr1:63773661-63774073 | Common:1; Rare:76 | ||||
chr1:66924795-66925036 | Common:1; Rare:104 | ||||
chr1:66925164-66925382 | Common:2; Rare:72 | ||||
chr1:67684878-67685541 | Common:3; Rare:192 | ||||
chr1:67833760-67834063 | Common:1; Rare:60 | ||||
chr1:70205391-70205770 | Rare:135 | ||||
chr1:70221271-70221840 | Rare:215 |