chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X135474234135474235TA9GENICheterozygous130203191
X135479688135479689CT15GENIChomozygous108428249
X135479724135479725CG13GENIChomozygous108530342
X135479742135479743AG11GENIChomozygous108530344
X135479760135479761AG9GENIChomozygous108821376
X135490390135490390T6GENIChomozygous129793860
X135479729135479730CG12GENIChomozygous108344209
X135479731135479732CG12GENIChomozygous108344211
X135479754135479755AG11GENIChomozygous108680816
X135479783135479784GC6GENIChomozygous120013139
X135479788135479789GC6GENIChomozygous120013140
X135479789135479790GC6GENIChomozygous120013141
X135479791135479792GC6GENIChomozygous120013142
X135479794135479795GC6GENIChomozygous120013143
X135479786135479787TC6GENIChomozygous108553313
X135479817135479818GC6GENIChomozygous108655314
X135490370135490370G4GENIChomozygous129793857
X135490380135490380T5GENIChomozygous129793858
X135490385135490386G5GENIChomozygous129793859
X135490410135490411A5GENIChomozygous129793861
X135490439135490440C6GENIChomozygous129793862
X135507659135507660C3GENIChomozygous129793864