Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44739667-44739935 | Common:2; Rare:106 | ||||
chr1:44775484-44775603 | Rare:48 | ||||
chr1:44775758-44776147 | Common:2; Rare:141 | ||||
chr1:44800175-44800380 | Common:1; Rare:45 | ||||
chr1:44801781-44801804 | Rare:9 | ||||
chr1:44808258-44808581 | Common:2; Rare:71 | ||||
chr1:44811259-44811345 | Rare:21 | ||||
chr1:44811761-44812041 | Common:1; Rare:61 | ||||
chr1:44986501-44986729 | Common:3; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
chr1:45011818-45012280 | Common:6; Rare:123; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45012638-45013007 | Common:1; Rare:103 | ||||
chr1:45339686-45339768 | Rare:18 | ||||
chr1:45339986-45340243 | Rare:92; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:45340388-45340577 | Common:1; Rare:46; Clinvar:1 | ||||
chr1:45491156-45491391 | Common:1; Rare:60 |