chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4139634593139634594GT20GENIChomozygous112853986
4139634793139634794AC12GENIChomozygous112853988
4139634845139634846AG19GENIChomozygous112853990
4139635066139635067GA13GENIChomozygous113056190
4139635106139635107CT17GENIChomozygous112853992
4139635679139635680GA15GENIChomozygous112853994
4139635691139635692GA11GENIChomozygous113056192
4139635773139635774GA28GENIChomozygous112853996
4139636407139636408AC19GENIChomozygous112854000
4139636493139636494CT23GENIChomozygous113056194
4139636693139636694GA16GENIChomozygous113056196
4139636961139636962TC18GENIChomozygous113056198
4139637580139637581TG19GENIChomozygous113056200
4139639146139639147CT7GENICheterozygous126053452
4139639468139639469GT14GENIChomozygous113056202
4139641222139641223CA26GENIChomozygous113056204
4139641628139641629CT18GENIChomozygous113056206
4139643716139643717GA20GENIChomozygous112854042
4139646425139646426GA14GENIChomozygous113056208
4139646503139646504GA13GENIChomozygous113056210
4139646795139646796TC17GENIChomozygous112854052
4139647217139647218AG13GENIChomozygous112854056
4139647780139647781CT24GENIChomozygous113056212
4139650010139650011TC17GENIChomozygous112854066
4139650839139650840AG9GENIChomozygous112854072
4139652442139652443TC11GENIChomozygous112854076
4139656723139656724CG28GENIChomozygous113056216
4139662514139662515GA14GENIChomozygous113056218