Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:219206683-219206909 | Rare:86 | ||||
chr2:219229586-219229887 | Common:1; Rare:87 | ||||
chr2:219245401-219245531 | Rare:36 | ||||
chr2:219279203-219279440 | Common:2; Rare:75 | ||||
chr2:219419845-219420155 | Common:2; Rare:63; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr2:219498663-219498938 | Common:2; Rare:62 | ||||
chr2:223957196-223957468 | Common:4; Rare:101 | ||||
chr2:226835889-226836068 | Rare:73 | ||||
chr2:227325191-227325355 | Common:5; Rare:56 | ||||
chr2:229921942-229922508 | Common:3; Rare:197 | ||||
chr2:231710266-231710481 | Common:1; Rare:102 | ||||
chr2:231961646-231961754 | Rare:30; Clinvar:1 | ||||
chr2:232550545-232550721 | Rare:69 | ||||
chr2:233854523-233854720 | Common:4; Rare:45 | ||||
chr2:237085769-237085955 | Common:2; Rare:70 |