Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:77697862-77698043 | Rare:37 | ||||
chr1:77885583-77885677 | Rare:18 | ||||
chr1:77889393-77889437 | Rare:10 | ||||
chr1:77899722-77899784 | Rare:13 | ||||
chr1:77899890-77899919 | Rare:4 | ||||
chr1:77915885-77916130 | Rare:59; Clinvar:3; Clinvar (benign):4 | ||||
chr1:77919160-77919200 | Rare:5 | ||||
chr1:77966889-77967050 | Common:1; Rare:44 | ||||
chr1:78012871-78013123 | Common:3; Rare:55 | ||||
chr1:83982992-83983029 | Rare:7 | ||||
chr1:85257970-85258282 | Common:5; Rare:75 | ||||
chr1:85275748-85275788 | Rare:8 | ||||
chr1:85314741-85315070 | Rare:51 | ||||
chr1:85340780-85340819 | Rare:9 | ||||
chr1:85423494-85423737 | Common:1; Rare:43 |