Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:31324005-31324318 | Common:1; Rare:88 | ||||
chr12:31326078-31326462 | Common:4; Rare:130 | ||||
chr12:31728995-31729292 | Common:1; Rare:91 | ||||
chr12:31959262-31959488 | Common:2; Rare:73 | ||||
chr12:32399196-32399587 | Common:5; Rare:111 | ||||
chr12:32755853-32756008 | Rare:57 | ||||
chr12:32896693-32897045 | Common:4; Rare:116; Clinvar:6; Clinvar (benign):7 | ||||
chr12:38905517-38905794 | Common:5; Rare:76 | ||||
chr12:39619795-39619919 | Common:1; Rare:24 | ||||
chr12:40224775-40225080 | Common:5; Rare:76; Clinvar (benign):1 | ||||
chr12:42238195-42238481 | Rare:100 | ||||
chr12:42325988-42326205 | Common:1; Rare:68 | ||||
chr12:42483914-42484190 | Common:1; Rare:39 | ||||
chr12:43758745-43758996 | Common:2; Rare:69; Clinvar:2 | ||||
chr12:43806241-43806385 | Common:2; Rare:50 |