Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:75511585-75511729 | Rare:49 | ||||
chr12:76763936-76764261 | Common:4; Rare:135 | ||||
chr12:79691006-79691255 | Common:1; Rare:88 | ||||
chr12:79934924-79935281 | Common:1; Rare:142 | ||||
chr12:82358372-82358529 | Rare:64 | ||||
chr12:82358736-82358887 | Common:3; Rare:79 | ||||
chr12:84912749-84912892 | Common:1; Rare:28 | ||||
chr12:85280143-85280481 | Common:3; Rare:120; Clinvar:1; Clinvar (benign):1 | ||||
chr12:88142066-88142368 | Rare:83; Clinvar:3 | ||||
chr12:89352462-89352707 | Rare:72 | ||||
chr12:93441888-93442154 | Common:2; Rare:83 | ||||
chr12:93571738-93571902 | Common:6; Rare:63 | ||||
chr12:94459865-94460003 | Common:2; Rare:36 | ||||
chr12:95073472-95073720 | Common:1; Rare:83 | ||||
chr12:95217384-95217746 | Common:4; Rare:99 |