chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2215634360215634361AC14GENIChomozygous59391236
2215636025215636029TGTG----5GENICheterozygous62230650
2215639464215639465A-10GENIChomozygous59391239
2215639858215639859CCAA5GENICheterozygous60457359
2215640780215640781C-13GENIChomozygous59391243
2215642593215642594TC15GENIChomozygous60348288
2215643797215643798TC15GENIChomozygous59391244
2215643671215643672CT18GENIChomozygous62205078
2215644898215644899GA17GENIChomozygous62205080
2215645528215645529GA18GENIChomozygous62205082
2215645916215645917GA32GENIChomozygous62205084
2215647135215647136TC31GENIChomozygous60237111
2215649293215649294CT22GENIChomozygous59391246
2215650554215650555TTTTTTTTTC5GENICheterozygous61268507
2215650614215650615GC11GENIChomozygous59391249
2215650843215650844AAGAGAGAGAGAGAGAAAGG2GENIChomozygous60457361
2215651028215651031AAA---20GENIChomozygous60548692
2215651847215651848CA19GENIChomozygous62205090
2215650081215650082GA27GENIChomozygous62205086
2215651037215651038AG23GENIChomozygous62205088
2215652924215652925TC19GENIChomozygous60348315
2215655598215655599A-8GENICheterozygous60561564
2215656694215656695CCT13GENICheterozygous61773569
2215656695215656696T-13GENICpossibly homozygous60348323
2215656709215656710T-17GENICpossibly homozygous62205092
2215656728215656733TTTTT-----10GENIChomozygous62205094
2215656741215656742TG10GENIChomozygous60516724
2215658875215658876CT22GENIChomozygous62205096
2215659480215659481AG21GENIChomozygous62205098
2215660079215660080AC22GENIChomozygous59391260
2215662576215662577AT10GENIChomozygous60348333
2215662856215662857GA11GENIChomozygous59391263
2215663536215663537TTAAA4GENICheterozygous61126836
2215663536215663537TTA4GENICheterozygous60759208
2215664588215664589GA20GENIChomozygous62205100
2215665344215665345CT26GENIChomozygous62205102