Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:213015191-213015681 | Rare:129 | ||||
chr1:213015685-213015942 | Rare:77 | ||||
chr1:213051113-213051351 | Common:1; Rare:72 | ||||
chr1:214280898-214281270 | Common:4; Rare:145 | ||||
chr1:214281386-214281683 | Common:4; Rare:132 | ||||
chr1:214551694-214551890 | Common:2; Rare:75 | ||||
chr1:214602891-214603313 | Common:4; Rare:120 | ||||
chr1:214603408-214603541 | Common:2; Rare:29 | ||||
chr1:215567368-215567529 | Rare:53 | ||||
chr1:215567691-215567843 | Common:1; Rare:47 | ||||
chr1:217630994-217631391 | Common:3; Rare:119 | ||||
chr1:218284955-218285393 | Common:5; Rare:153 | ||||
chr1:218345924-218346100 | Common:5; Rare:60; Clinvar:8; Clinvar (benign):3 | ||||
chr1:219173734-219173965 | Common:2; Rare:128 | ||||
chr1:220046302-220046828 | Common:1; Rare:158 |