Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:893158-893484 | Common:3; Rare:139 | ||||
chr19:913149-913274 | Rare:40 | ||||
chr19:984182-984392 | Common:4; Rare:79 | ||||
chr19:1103794-1104126 | Common:4; Rare:139 | ||||
chr19:1132125-1132366 | Common:1; Rare:109 | ||||
chr19:1605369-1605665 | Common:3; Rare:114 | ||||
chr19:1622165-1622363 | Rare:78 | ||||
chr19:2328554-2328703 | Common:2; Rare:71 | ||||
chr19:2456674-2457080 | Common:2; Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
chr19:2783250-2783488 | Rare:84 | ||||
chr19:2944916-2945175 | Common:5; Rare:90 | ||||
chr19:3062770-3062995 | Common:3; Rare:89 | ||||
chr19:3366470-3366639 | Common:3; Rare:46 | ||||
chr19:3606853-3606920 | Rare:17 | ||||
chr19:3761613-3761752 | Common:2; Rare:43 |