chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1100594235100594236GA11INTERGENICpossibly homozygous61483181
1100594971100594972AG20INTERGENICpossibly homozygous61483182
1100595780100595781A-3GENICheterozygous61483183
1100596863100596864AG11GENICheterozygous61483187
1100596900100596901GC15GENIChomozygous61483188
1100597622100597623AC19GENICpossibly homozygous61483189
1100600642100600643TC7GENIChomozygous61483191
1100601209100601210GA9GENICpossibly homozygous61483193
1100601288100601289AG12GENIChomozygous61483194
1100601438100601439CT5GENIChomozygous61483195
1100601502100601503GA6GENIChomozygous61483196
1100601512100601515AAA---4GENIChomozygous61483197
1100601761100601762GA8GENICpossibly homozygous61483198
1100601830100601831CT14GENIChomozygous61483199
1100602150100602151GA16GENICpossibly homozygous61483200
1100602442100602443AATC3GENIChomozygous61483201
1100602509100602510TC11GENICpossibly homozygous61483202
1100602689100602690GA14GENICpossibly homozygous61483203
1100604705100604706AC22GENIChomozygous61483205
1100605232100605233CT29GENICpossibly homozygous61483206
1100606549100606550AG22GENICpossibly homozygous61483207
1100607037100607038TG10GENICpossibly homozygous61483208