Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23778189-23778521 | Common:26; Rare:401 | ||||
chr1:23790959-23791257 | Rare:211 | ||||
chr1:23800668-23801165 | Common:3; Rare:351 | ||||
chr1:23825325-23825627 | Common:5; Rare:153; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
chr1:23838550-23838791 | Common:6; Rare:125 | ||||
chr1:23868216-23868531 | Common:6; Rare:88; Clinvar:2; Clinvar (benign):5 | ||||
chr1:23958972-23959419 | Common:10; Rare:204 | ||||
chr1:23959482-23959856 | Common:10; Rare:232 | ||||
chr1:23960527-23960697 | Common:1; Rare:34 | ||||
chr1:23980179-23980605 | Common:1; Rare:293 | ||||
chr1:24187224-24187544 | Common:10; Rare:119 | ||||
chr1:24319212-24319494 | Common:1; Rare:61 | ||||
chr1:24319433-24319645 | Common:1; Rare:82 | ||||
chr1:24322250-24322600 | Common:4; Rare:136 | ||||
chr1:24413120-24413560 | Common:7; Rare:156 |