Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207321625-207322033 | Rare:96 | ||||
chr1:207322127-207322318 | Rare:63 | ||||
chr1:207751765-207752305 | Common:3; Rare:166; Clinvar:1 | ||||
chr1:208243878-208244050 | Rare:38 | ||||
chr1:208244249-208244461 | Common:1; Rare:62 | ||||
chr1:209652341-209652618 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
chr1:209675198-209675518 | Common:3; Rare:82 | ||||
chr1:209784679-209784915 | Common:4; Rare:62 | ||||
chr1:209805471-209805661 | Common:2; Rare:32 | ||||
chr1:209805957-209806299 | Common:5; Rare:98; Clinvar:3; Clinvar (benign):2 | ||||
chr1:211259075-211259399 | Common:1; Rare:104 | ||||
chr1:211326747-211326874 | Common:3; Rare:30 | ||||
chr1:211578253-211578486 | Rare:53 | ||||
chr1:212035507-212035793 | Common:2; Rare:72 | ||||
chr1:212285072-212285449 | Common:3; Rare:125 |