chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
44916052349160524GC36GENIChomozygous56872186
44916055249160553CT34GENIChomozygous56872189
44916138849161389GA40GENIChomozygous56872191
44916168949161690G-42GENIChomozygous56872194
44916210449162107AAA---55GENIChomozygous56872197
44916239949162400GA61GENIChomozygous56872199
44916242649162429TTT---16GENICheterozygous56872201
44916242749162429TT--16GENICheterozygous57316863
44916254149162542T-67GENIChomozygous56872204
44916303049163031AG43GENIChomozygous56872206
44916367849163679AG82GENIChomozygous56872209
44916368949163690GGT72GENIChomozygous56872212
44916421549164216CCT71GENIChomozygous56872215
44916451549164516AG62GENIChomozygous56872218
44916471349164714GA73GENIChomozygous56872219
44916481649164817AG51GENICheterozygous57316865
44916498249164983GT105GENIChomozygous56872222
44916520449165205T-69GENIChomozygous56872224
44916536349165364TTA64GENIChomozygous56872227
44916569249165693TC58GENIChomozygous56872230
44916695949166965GTGTGT------21GENICheterozygous56872233
44916696149166965GTGT----21GENICheterozygous56872236
44916696349166965GT--21GENICheterozygous57316867
44916718049167181GGA55GENIChomozygous56872239
44916786249167863CT62GENICpossibly homozygous56872242
44916944149169442GT40GENIChomozygous56872245
44917144049171441GGA59GENICpossibly homozygous56872248
44917267749172678AC56GENIChomozygous56872250
44917298749172988AT66GENICpossibly homozygous56872253
44917409849174099T-52GENIChomozygous56872256
44917564449175645GGA29GENIChomozygous56872259
44917721649177217GGA58GENIChomozygous56872264
44917723249177233AG62GENIChomozygous56872267