Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:87342607-87342920 | Common:1; Rare:80 | ||||
chr10:87862258-87862584 | Rare:155; Clinvar:1 | ||||
chr10:88941227-88941531 | Common:2; Rare:59; Clinvar:5; Clinvar (benign):4 | ||||
chr10:89283579-89283750 | Rare:24 | ||||
chr10:89516195-89516363 | Common:1; Rare:33 | ||||
chr10:90915775-90916130 | Common:2; Rare:85; Clinvar:6; Clinvar (benign):2 | ||||
chr10:90917724-90917986 | Rare:62; Clinvar:3 | ||||
chr10:90918348-90918449 | Common:2; Rare:23 | ||||
chr10:90920097-90920556 | Rare:128; Clinvar:10; Clinvar (benign):6 | ||||
chr10:90935569-90935785 | Common:1; Rare:42 | ||||
chr10:91162468-91162492 | Rare:4 | ||||
chr10:91551937-91552156 | Common:2; Rare:35 | ||||
chr10:91589723-91589903 | Common:3; Rare:22 | ||||
chr10:91807502-91807536 | Rare:12 | ||||
chr10:92240646-92240803 | Rare:34 |