chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2200704020200704021AG18GENIChomozygous59926957
2200704134200704135CG31GENIChomozygous59926958
2200704204200704205AG35GENIChomozygous59926959
2200704365200704366CG26GENIChomozygous59338464
2200704406200704407GA23GENIChomozygous59338465
2200704431200704434TCG---26GENIChomozygous59338466
2200704440200704441CT26GENIChomozygous59338468
2200704448200704449CT26GENIChomozygous59338469
2200704703200704704TC25GENIChomozygous59926960
2200704897200704898TTA30GENIChomozygous59338473
2200705277200705278CT37GENIChomozygous59338474
2200705318200705319TG30GENIChomozygous59338475
2200705704200705705GA32GENIChomozygous59338476
2200705771200705772CT42GENIChomozygous59338477
2200706049200706050CT38GENIChomozygous59338478
2200706132200706133GA25GENIChomozygous59926961
2200706402200706403GA38GENIChomozygous59926962
2200706465200706466CT31GENIChomozygous59338480
2200707244200707245AC30GENIChomozygous59338483
2200707267200707268TC32GENIChomozygous59338484
2200707453200707454TC21GENIChomozygous59338485
2200707516200707517AAG23GENIChomozygous59338486
2200707555200707557AT--28GENIChomozygous59338487
2200707941200707942GA39GENIChomozygous59338488
2200708010200708011GA28GENIChomozygous59338489
2200708090200708091AG36GENIChomozygous59338490
2200708685200708686GA23GENIChomozygous59338493
2200709009200709017CACTCACT--------6GENICheterozygous60512719
2200709547200709548AT32GENIChomozygous59926965
2200709648200709649CA22GENIChomozygous59338498
2200709695200709696TC21GENIChomozygous59338499
2200709717200709718GA26GENIChomozygous59926966
2200709733200709734GA32GENIChomozygous59338501
2200709736200709737CT32GENIChomozygous59338502
2200709788200709789GA33GENIChomozygous59338503
2200709814200709815CA17GENIChomozygous59338504
2200710332200710333T-34GENIChomozygous59926967
2200710345200710346GA36GENIChomozygous59338506
2200710436200710437TC35GENIChomozygous59338508
2200710805200710806AC40GENICpossibly homozygous59926968