Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154970031-154970512 | Common:1; Rare:151 | ||||
chr1:154970514-154970543 | Rare:8 | ||||
chr1:154970631-154971057 | Common:2; Rare:88 | ||||
chr1:154971084-154971285 | Rare:33 | ||||
chr1:154973631-154973930 | Rare:74 | ||||
chr1:154974322-154974817 | Rare:124 | ||||
chr1:154974901-154975137 | Common:3; Rare:83 | ||||
chr1:154975213-154975588 | Common:1; Rare:63 | ||||
chr1:154975757-154976071 | Common:1; Rare:63 | ||||
chr1:154983110-154983402 | Common:2; Rare:58; Clinvar (benign):1 | ||||
chr1:154983723-154983839 | Rare:37 | ||||
chr1:155002110-155002310 | Common:1; Rare:52 | ||||
chr1:155002483-155002853 | Common:2; Rare:60 | ||||
chr1:155051118-155051406 | Common:2; Rare:98 | ||||
chr1:155063601-155063775 | Rare:51 |