Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23368181-23368485 | Common:1; Rare:89 | ||||
chr1:23368769-23368989 | Common:2; Rare:69 | ||||
chr1:23369367-23369602 | Rare:113 | ||||
chr1:23484177-23484513 | Common:1; Rare:98 | ||||
chr1:23691740-23691847 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
chr1:23692872-23692932 | Common:1; Rare:15 | ||||
chr1:23778239-23778451 | Common:6; Rare:109 | ||||
chr1:23791842-23791995 | Rare:31 | ||||
chr1:23825354-23825534 | Common:3; Rare:62; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr1:23959635-23959946 | Common:2; Rare:78 | ||||
chr1:23975195-23975411 | Common:1; Rare:47 | ||||
chr1:23978647-23978925 | Common:1; Rare:23 | ||||
chr1:23980273-23980510 | Rare:76 | ||||
chr1:24187246-24187310 | Common:1; Rare:16 | ||||
chr1:24319220-24319526 | Common:1; Rare:71 |