Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45500054-45500358 | Common:1; Rare:74; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521880-45522034 | Common:1; Rare:58 | ||||
chr1:45550563-45550883 | Common:2; Rare:78 | ||||
chr1:45583927-45584051 | Rare:45 | ||||
chr1:45687057-45687350 | Common:1; Rare:76 | ||||
chr1:45688055-45688241 | Common:1; Rare:53 | ||||
chr1:46303315-46303715 | Common:2; Rare:102 | ||||
chr1:46340481-46340773 | Common:5; Rare:67 | ||||
chr1:46340939-46341343 | Common:3; Rare:95 | ||||
chr1:46604200-46604412 | Common:1; Rare:56 | ||||
chr1:46616809-46616984 | Common:2; Rare:40 | ||||
chr1:48776712-48776841 | Rare:30 | ||||
chr1:51729666-51729897 | Common:2; Rare:64 | ||||
chr1:51878316-51878344 | Rare:11 | ||||
chr1:51878682-51879031 | Common:1; Rare:102 |