Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:85276321-85276580 | Common:4; Rare:87; Clinvar (benign):3 | ||||
chr1:85707878-85708213 | Common:1; Rare:97 | ||||
chr1:86704478-86704627 | Rare:53 | ||||
chr1:86704708-86704966 | Common:3; Rare:93 | ||||
chr1:86914325-86914752 | Common:1; Rare:128 | ||||
chr1:87328549-87328948 | Common:3; Rare:151 | ||||
chr1:87329010-87329036 | Rare:10 | ||||
chr1:88992591-88992984 | Common:3; Rare:101 | ||||
chr1:89022718-89022897 | Rare:32 | ||||
chr1:89198872-89198995 | Rare:15 | ||||
chr1:89632900-89633156 | Rare:70 | ||||
chr1:89994981-89995218 | Common:2; Rare:89 | ||||
chr1:92298943-92299074 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
chr1:93079097-93079310 | Common:2; Rare:89 | ||||
chr1:93179866-93179935 | Common:1; Rare:17 |