Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:41921115-41921255 | Rare:37 | ||||
chr6:42050356-42050534 | Common:1; Rare:51 | ||||
chr6:42746073-42746352 | Rare:75 | ||||
chr6:42879583-42879940 | Rare:103 | ||||
chr6:42929249-42929541 | Common:3; Rare:78 | ||||
chr6:42984304-42984619 | Rare:79 | ||||
chr6:43013875-43014280 | Common:2; Rare:88 | ||||
chr6:43059812-43059880 | Rare:23 | ||||
chr6:43182071-43182191 | Rare:29 | ||||
chr6:43516858-43517112 | Common:4; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
chr6:43575990-43576227 | Common:1; Rare:90; Clinvar:8 | ||||
chr6:43769979-43770221 | Common:6; Rare:63 | ||||
chr6:44127356-44127639 | Common:4; Rare:80 | ||||
chr6:44387455-44387738 | Common:4; Rare:72 | ||||
chr6:47478067-47478232 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):3 |