chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32124535321245354GA19GENIChomozygous149313514
32124924421249245CT10GENIChomozygous147431363
32125746121257462TG20GENIChomozygous149313515
32124889621248897AG17GENIChomozygous136653419
32125524321255244TC16GENIChomozygous136653423
32124898521248985T26GENIChomozygous136551787
32125330921253309CG24GENIChomozygous149308614
32125333121253331CT24GENIChomozygous149308615
32125674421256748TTTG21GENIChomozygous149308616
32126032021260321TA12GENIChomozygous149313516
32126244021262446AAGAGA29GENIChomozygous149308617
32126320021263200A20GENIChomozygous136551790
32126647121266472TC27GENIChomozygous136653427
32126686921266869GGTTGGTTGATTGGTT13GENIChomozygous136551791
32126772821267729TA10GENIChomozygous136653429
32126783321267834TC11GENIChomozygous149313517
32127218121272182CT17GENIChomozygous149313518
32127235521272356GA16GENIChomozygous136653430
32127489521274896GA16GENIChomozygous149313519
32127972521279726CT14GENIChomozygous145399919
32128104021281041AG24GENIChomozygous149313520
32126782021267821T11GENICheterozygous149487944
32124902121249022A26GENICheterozygous136551788
32124902121249022AT26GENICpossibly homozygous154072461