Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11934553-11934754 | Common:3; Rare:66; Clinvar:5; Clinvar (benign):1 | ||||
chr1:11980086-11980473 | Common:6; Rare:125; Clinvar:1; Clinvar (benign):4 | ||||
chr1:12618133-12618464 | Common:3; Rare:69 | ||||
chr1:13749191-13749460 | Common:2; Rare:97 | ||||
chr1:15526575-15526917 | Common:2; Rare:109 | ||||
chr1:15757804-15757921 | Common:1; Rare:26 | ||||
chr1:15758725-15758817 | Common:1; Rare:20 | ||||
chr1:16237143-16237339 | Rare:63 | ||||
chr1:16352401-16352591 | Common:3; Rare:105 | ||||
chr1:16440522-16440780 | Common:2; Rare:78 | ||||
chr1:16613508-16613645 | |||||
chr1:16921807-16921941 | Rare:21 | ||||
chr1:16992063-16992251 | Rare:57; Clinvar:1 | ||||
chr1:17053953-17054239 | Common:3; Rare:93; Clinvar:16; Clinvar (benign):11 | ||||
chr1:17119449-17119558 | Rare:28 |