chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4245048501245048502GA13GENICpossibly homozygous57188204
4245048813245048814TC23GENIChomozygous57188206
4245049011245049012CT19GENIChomozygous57188208
4245049712245049713AC11GENIChomozygous57188210
4245051657245051658AC24GENIChomozygous57188222
4245052063245052064CG23GENIChomozygous57188224
4245052436245052437TC27GENICpossibly homozygous57188226
4245055602245055603GA24GENICpossibly homozygous57188228
4245056945245056946GA19GENIChomozygous57188234
4245058113245058114CT22GENIChomozygous57188236
4245058504245058505TA13GENICpossibly homozygous57188238
4245059862245059863GA6GENICheterozygous57188240
4245060226245060227A-3GENICheterozygous57188242
4245060819245060820AG15GENIChomozygous57188244
4245063320245063321TTAAAAAAA2GENICheterozygous58493357
4245065712245065713GA27GENICpossibly homozygous57188246
4245067173245067174A-2GENICheterozygous57188248
4245067820245067821C-9GENICheterozygous57188252