chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7759873759874TA63GENIChomozygous146439549
7760483760484GA66GENIChomozygous146439550
7761528761529AT5GENIChomozygous403198077
7761528761529A5GENICheterozygous403198078
7767299767300GA58GENIChomozygous141924883
7770182770183GC73GENIChomozygous137986996
7771235771236AT45GENICheterozygous154420100
7771235771236A45GENICpossibly homozygous403198081
7772422772423TA53GENIChomozygous146439551
7772578772579T52GENICheterozygous403770824
7772578772579TG52GENICheterozygous403770825
7772579772580T52GENICheterozygous403770826
7772579772580TG52GENICheterozygous403770827
7771183771183T47GENICpossibly homozygous141904762
7766727766727A30GENICpossibly homozygous137932315
7769544769544T41GENICpossibly homozygous137932316
7774044774045AG57GENIChomozygous137986998
7777246777247AG6GENIChomozygous147436130
7777263777264GA7GENICpossibly homozygous141924892
7777273777274AG7GENICpossibly homozygous147436131
7777290777291GA7GENICpossibly homozygous141924893
7777297777298AG7GENICpossibly homozygous147436132
7777348777349AG9GENICheterozygous404076428
7777334777335T8GENICheterozygous404076425
7777334777335TA8GENICheterozygous404076426
7777348777349A9GENICheterozygous404076427
7777714777715CT6GENIChomozygous404076429
7777714777715C6GENICheterozygous404076430
7779675779680AGTCA68GENIChomozygous146434030
7779682779682TTCCCTGAGAAG70GENIChomozygous146434031
7779903779904CT65GENIChomozygous137987003
7780886780887CT66GENIChomozygous146439552
7785542785543AG63GENIChomozygous137987005
7785836785837AG60GENIChomozygous137987006
7785873785874CT55GENIChomozygous137987008
7785926785927AC55GENIChomozygous146439553
7788435788436CT67GENIChomozygous146439554
7790985790986AG53GENIChomozygous137987014