Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:226062470-226062725 | Rare:75 | ||||
chr1:226063267-226063542 | Common:2; Rare:76 | ||||
chr1:226186631-226186848 | Common:1; Rare:75 | ||||
chr1:226309103-226309370 | Common:1; Rare:118 | ||||
chr1:226309490-226309842 | Common:9; Rare:249 | ||||
chr1:226407921-226408255 | Common:3; Rare:102 | ||||
chr1:226548492-226548892 | Rare:174 | ||||
chr1:226737659-226737936 | Rare:78 | ||||
chr1:226739248-226739439 | Common:4; Rare:42 | ||||
chr1:226870453-226870621 | Common:1; Rare:49; Clinvar (benign):1 | ||||
chr1:226870785-226870898 | Rare:26 | ||||
chr1:226939665-226939788 | Rare:33 | ||||
chr1:226939887-226940323 | Common:2; Rare:140; Clinvar:2 | ||||
chr1:227317569-227317815 | Common:1; Rare:60 | ||||
chr1:227318041-227318740 | Common:11; Rare:240 |