Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:46335643-46335760 | Common:1; Rare:48; Clinvar:4; Clinvar (benign):5 | ||||
chr22:46626291-46626392 | Common:1; Rare:25 | ||||
chr22:46762496-46762669 | Common:3; Rare:64 | ||||
chr22:50244949-50245111 | Common:2; Rare:62 | ||||
chr22:50582794-50583142 | Common:7; Rare:114; Clinvar:2; Clinvar (benign):3 | ||||
chr22:50628107-50628276 | Common:9; Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
chr22:50782426-50782455 | Rare:5 | ||||
chr22:50783601-50783859 | Common:2; Rare:79 | ||||
chr3:3126813-3126984 | Common:4; Rare:74; Clinvar (benign):1 | ||||
chr3:4303075-4303502 | Common:3; Rare:132 | ||||
chr3:4493177-4493348 | Rare:60 | ||||
chr3:4979411-4979741 | Common:2; Rare:82 | ||||
chr3:5187339-5187663 | Common:5; Rare:131 | ||||
chr3:8501653-8501854 | Rare:69 | ||||
chr3:9363007-9363098 | Rare:32 |