Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:88882013-88882298 | Common:2; Rare:74 | ||||
chr1:88997921-88998246 | Common:2; Rare:42 | ||||
chr1:89855382-89855594 | Common:1; Rare:30 | ||||
chr1:89931035-89931046 | |||||
chr1:89950927-89950965 | Rare:10 | ||||
chr1:90022184-90022342 | Rare:34 | ||||
chr1:91387379-91387553 | Common:2; Rare:14 | ||||
chr1:91642685-91642998 | Common:1; Rare:99 | ||||
chr1:92074260-92074452 | Rare:33 | ||||
chr1:92275286-92275314 | Rare:5 | ||||
chr1:92645557-92645658 | Rare:11 | ||||
chr1:92649024-92649105 | Rare:18 | ||||
chr1:92649443-92649651 | Common:2; Rare:43 | ||||
chr1:92744845-92745091 | Common:1; Rare:36 | ||||
chr1:92833394-92833522 | Rare:35; Clinvar (pathogenic):1 |