Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:42564208-42564318 | Rare:29 | ||||
chr6:42564380-42564404 | Rare:6 | ||||
chr6:42746069-42746360 | Rare:79 | ||||
chr6:42746502-42746790 | Rare:70 | ||||
chr6:42746808-42747012 | Rare:40 | ||||
chr6:42747054-42747295 | Rare:57 | ||||
chr6:42781971-42782091 | Common:2; Rare:27 | ||||
chr6:42879577-42879940 | Rare:106 | ||||
chr6:42890786-42890929 | Rare:57 | ||||
chr6:42929085-42929566 | Common:4; Rare:139 | ||||
chr6:42979171-42979324 | Common:3; Rare:47; Clinvar:4; Clinvar (benign):1 | ||||
chr6:42984276-42984635 | Rare:93 | ||||
chr6:43013391-43013550 | Common:1; Rare:44 | ||||
chr6:43013809-43014329 | Common:2; Rare:130 | ||||
chr6:43053820-43053963 | Common:1; Rare:48; Clinvar:5 |