chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
44916052349160524GC11GENIChomozygous56872186
44916055249160553CT13GENIChomozygous56872189
44916138849161389GA17GENIChomozygous56872191
44916168949161690G-14GENIChomozygous56872194
44916210449162107AAA---14GENIChomozygous56872197
44916239949162400GA7GENIChomozygous56872199
44916254149162542T-17GENIChomozygous56872204
44916303049163031AG21GENIChomozygous56872206
44916367849163679AG23GENIChomozygous56872209
44916368949163690GGT22GENIChomozygous56872212
44916421549164216CCT12GENIChomozygous56872215
44916451549164516AG17GENIChomozygous56872218
44916471349164714GA17GENIChomozygous56872219
44916498249164983GT14GENIChomozygous56872222
44916536349165364TTA18GENIChomozygous56872227
44916569249165693TC13GENIChomozygous56872230
44916718049167181GGA14GENIChomozygous56872239
44916786249167863CT16GENIChomozygous56872242
44916944149169442GT14GENIChomozygous56872245
44917144049171441GGA11GENICpossibly homozygous56872248
44917267749172678AC16GENIChomozygous56872250
44917298749172988AT16GENIChomozygous56872253
44917409849174099T-9GENIChomozygous56872256
44917721649177217GGA13GENIChomozygous56872264
44917723249177233AG15GENIChomozygous56872267
44916520349165204T-13GENIChomozygous60036408