chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4139633457139633458GA13GENIChomozygous113056186
4139633534139633535CA18GENIChomozygous113056188
4139634593139634594GT29GENIChomozygous112853986
4139634793139634794AC33GENIChomozygous112853988
4139634845139634846AG24GENIChomozygous112853990
4139635066139635067GA33GENIChomozygous113056190
4139635106139635107CT30GENIChomozygous112853992
4139635679139635680GA26GENIChomozygous112853994
4139635691139635692GA30GENIChomozygous113056192
4139635773139635774GA33GENIChomozygous112853996
4139636407139636408AC25GENIChomozygous112854000
4139636493139636494CT30GENIChomozygous113056194
4139636693139636694GA35GENIChomozygous113056196
4139636961139636962TC35GENIChomozygous113056198
4139637482139637483CT22GENIChomozygous112854002
4139637580139637581TG14GENIChomozygous113056200
4139639468139639469GT27GENIChomozygous113056202
4139641222139641223CA31GENIChomozygous113056204
4139641628139641629CT22GENIChomozygous113056206
4139643716139643717GA19GENIChomozygous112854042
4139644140139644141CT24GENIChomozygous113387752
4139646425139646426GA15GENIChomozygous113056208
4139646503139646504GA22GENIChomozygous113056210
4139646795139646796TC17GENIChomozygous112854052
4139647780139647781CT19GENIChomozygous113056212
4139650010139650011TC21GENIChomozygous112854066
4139652442139652443TC23GENIChomozygous112854076
4139656723139656724CG33GENIChomozygous113056216
4139662514139662515GA31GENIChomozygous113056218