Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42463003-42463318 | Common:4; Rare:93 | ||||
chr1:42658286-42658452 | Common:2; Rare:47 | ||||
chr1:42682158-42682435 | Common:2; Rare:70 | ||||
chr1:42683228-42683465 | Common:3; Rare:106 | ||||
chr1:42767010-42767303 | Common:4; Rare:92; Clinvar (benign):1 | ||||
chr1:42817004-42817168 | Common:1; Rare:48 | ||||
chr1:42846406-42846638 | Common:1; Rare:62 | ||||
chr1:42958849-42959063 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):2 | ||||
chr1:43270946-43271020 | Rare:15 | ||||
chr1:43285557-43285712 | Common:2; Rare:28 | ||||
chr1:43358660-43358982 | Common:7; Rare:102 | ||||
chr1:43367937-43368197 | Rare:63 | ||||
chr1:43389757-43389950 | Common:3; Rare:86 | ||||
chr1:43649806-43650180 | Rare:85 | ||||
chr1:43946579-43946987 | Rare:108 |