Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40257915-40258255 | Common:4; Rare:87; Clinvar:6 | ||||
chr1:42335175-42335381 | Common:5; Rare:99 | ||||
chr1:42816981-42817136 | Common:1; Rare:43 | ||||
chr1:42958800-42959078 | Common:4; Rare:76; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43358662-43359006 | Common:7; Rare:110 | ||||
chr1:43367965-43368208 | Rare:67 | ||||
chr1:43389768-43389913 | Common:3; Rare:55 | ||||
chr1:44674421-44674749 | Common:3; Rare:85 | ||||
chr1:44775469-44775626 | Common:1; Rare:67 | ||||
chr1:45339978-45340178 | Rare:61 | ||||
chr1:45521856-45521972 | Common:1; Rare:48 | ||||
chr1:45687059-45687263 | Common:1; Rare:62 | ||||
chr1:46303264-46303289 | Rare:11 | ||||
chr1:46303315-46303745 | Common:2; Rare:114 | ||||
chr1:47333727-47333984 | Common:3; Rare:87 |