chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7759873759874TA64GENIChomozygous146439549
7760483760484GA44GENIChomozygous146439550
7761497761499AA7GENIChomozygous147352558
7766727766727A26GENICpossibly homozygous137932315
7767299767300GA33GENIChomozygous141924883
7769544769544T30GENIChomozygous137932316
7770182770183GC52GENIChomozygous137986996
7772422772423TA44GENIChomozygous146439551
7772579772580T24GENIChomozygous403770826
7771235771236AT21GENIChomozygous154420100
7761524761525TA9GENICheterozygous147353638
7761528761529AT8GENICheterozygous403198077
7761528761529A8GENICheterozygous403198078
7771235771236A21GENICheterozygous403198081
7771183771183T16GENICpossibly homozygous141904762
7772578772579T24GENIChomozygous403770824
7772578772579TG24GENICheterozygous403770825
7772579772580TG24GENICheterozygous403770827
7774044774045AG43GENIChomozygous137986998
7777246777247AG13GENIChomozygous147436130
7777263777264GA10GENIChomozygous141924892
7777273777274AG8GENIChomozygous147436131
7777290777291GA4GENIChomozygous141924893
7777297777298AG4GENIChomozygous147436132
7779903779904CT57GENIChomozygous137987003
7780886780887CT44GENIChomozygous146439552
7784045784046AG31GENICpossibly homozygous147353640
7785433785434CT36GENIChomozygous147353641
7785542785543AG51GENIChomozygous137987005
7785836785837AG48GENIChomozygous137987006
7785873785874CT43GENIChomozygous137987008
7785926785927AC36GENIChomozygous146439553
7788435788436CT44GENIChomozygous146439554
7790985790986AG47GENIChomozygous137987014
7779682779682TTCCCTGAGAAG51GENIChomozygous146434031
7779319779320TC10GENICheterozygous404546156
7779319779320T10GENICheterozygous404546157
7779319779320TA10GENICheterozygous404546158
7779675779680AGTCA51GENIChomozygous146434030