chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1241354610241354611T-28GENICheterozygous62315548
1241375655241375656GC33GENICheterozygous62811142
1241411610241411611T-50GENICheterozygous61134856
1241425877241425878TA40GENICheterozygous61623068
1241425954241425955GA37GENICheterozygous62107970
1241430544241430545CA46GENICheterozygous61134886
1241449739241449740GA39GENICheterozygous62107979
1241450662241450663TG41GENICheterozygous62107980
1241454938241454939GA23GENICheterozygous62107982
1241454946241454947CCA25GENICheterozygous61134929
1241455075241455076AT33GENICheterozygous61134930
1241455445241455455CAATTCAGCT----------53GENICheterozygous62881513
1241456980241456981AG37GENICheterozygous61134934
1241457075241457076AG36GENICheterozygous61134935
1241465593241465594AG17GENICheterozygous61623104
1241466523241466524CT58GENICheterozygous61623106
1241467424241467425AG21GENICheterozygous61134989
1241467461241467462AG24GENICheterozygous61134990
1241505264241505265AG68GENICheterozygous61135091
1241505662241505663A-29GENICheterozygous61135092
1241505725241505726GA27GENICheterozygous61135093
1241507473241507474CT34GENICheterozygous61135099
1241507506241507507GA16GENICheterozygous61135100
1241511123241511124AG19GENICheterozygous61135105
1241530168241530169AT36GENICheterozygous61135117
1241532843241532844GA16GENICheterozygous61135124
1241533836241533837GA21GENICheterozygous62881514
1241540505241540506AG8GENICheterozygous61623190