Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:46715713-46715908 | Common:1; Rare:42 | ||||
chr2:46743947-46743969 | Common:1; Rare:7 | ||||
chr2:46757787-46757997 | Rare:41 | ||||
chr2:46764017-46764057 | Common:1; Rare:10 | ||||
chr2:46777733-46778032 | Common:1; Rare:63 | ||||
chr2:46827548-46827896 | Common:4; Rare:98 | ||||
chr2:46849850-46850195 | Common:2; Rare:90 | ||||
chr2:46850782-46851098 | Common:2; Rare:67 | ||||
chr2:46855609-46855853 | Rare:52 | ||||
chr2:46878970-46879222 | Rare:43 | ||||
chr2:46905541-46905708 | Common:1; Rare:46; Clinvar:1 | ||||
chr2:46906546-46906622 | Common:1; Rare:18 | ||||
chr2:47162393-47162663 | Rare:55; Clinvar (benign):2 | ||||
chr2:47174835-47175288 | Common:6; Rare:130 | ||||
chr2:47175669-47175946 | Common:3; Rare:100 |