chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------35GENIChomozygous763353286
85378107053781071CT29GENIChomozygous660552233
85378121053781211AG14GENIChomozygous660552234
85378128753781288GGA10GENICheterozygous763353288
85378128753781288GGAA10GENICheterozygous763353289
85378128753781288GGAAA10GENICheterozygous763353290
85378133353781334AG22GENIChomozygous660552235
85378146653781467AG34GENIChomozygous660552236
85378180553781806AG28GENIChomozygous660552237
85378193153781932TTTA4GENICheterozygous763353291
85378193153781932TTTTA4GENICheterozygous763353292
85378193153781932TTTTTA4GENICheterozygous763353293
85378200853782013GTTTG-----11GENIChomozygous763353294
85378241353782414CT19GENIChomozygous660552238
85378260753782608TC15GENIChomozygous660552239
85378277053782771GA19GENIChomozygous660552240
85378331953783320AG54GENIChomozygous660552241
85378353253783533GGT23GENIChomozygous763353295
85378373853783739GT12GENIChomozygous660552242
85378379353783794TC21GENIChomozygous660552243
85378391753783918T-36GENICpossibly homozygous763353296
85378391953783926TGCGTGT-------45GENICpossibly homozygous763353297
85378404853784049TC34GENIChomozygous660552244
85378461253784613TC31GENIChomozygous660552245
85378550553785506T-1GENIChomozygous763353298
85378552153785522CCTTTCTT3GENIChomozygous763353301