chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172724423027244231CT28GENIChomozygous111184129
172724511427245115AC29GENIChomozygous111184131
172724592327245924GA21GENIChomozygous111184133
172724663727246638AG17GENIChomozygous111184135
172724687227246873TC30GENIChomozygous111184137
172724699127246992AG29GENIChomozygous111012589
172724713327247134CA20GENIChomozygous111184139
172724729627247297CT30GENIChomozygous111184141
172724730727247308AT32GENIChomozygous111184143
172724736727247368GA39GENIChomozygous111184145
172724738227247383TG38GENIChomozygous111184147
172724741527247416GA40GENIChomozygous111184149
172724750027247501GA18GENIChomozygous111184151
172724762527247626GT23GENIChomozygous111184153
172724812427248125TA26GENIChomozygous111184155
172724836127248362TC25GENIChomozygous111184157
172724860327248604AG17GENIChomozygous111012591
172724879627248797GA38GENIChomozygous111184159
172724920527249206AC27GENICpossibly homozygous111238456
172724924627249247AC29GENIChomozygous111238458
172724962427249625TC26GENIChomozygous111238460
172725067427250675TC26GENIChomozygous111184161
172725071527250716TC34GENIChomozygous111184163
172725074527250746CG38GENIChomozygous111184165
172725076627250767AG37GENIChomozygous111184167
172725090627250907TC27GENIChomozygous111184169
172725160227251603AG21GENIChomozygous111184171
172725169927251700AG20GENIChomozygous111184173
172725241427252415AG29GENIChomozygous111012593
172725243927252440AG29GENIChomozygous111238462
172725265427252655GA15GENIChomozygous111184175
172725266527252666CT19GENIChomozygous111238464
172725280927252810AG34GENIChomozygous111184177
172725293627252937TC28GENIChomozygous111184179
172726925127269252CT23GENIChomozygous111012597
172727050827270509GA36GENIChomozygous111184181
172727203827272039GA25GENIChomozygous111184185
172727274927272750GA14GENIChomozygous111184187
172727458027274581CT33GENIChomozygous111184189
172727487727274878CT15GENIChomozygous111184191
172727586427275865TA26GENIChomozygous111184193