chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
115709545257095453GA6GENIChomozygous138997461
115709545257095453G6GENICheterozygous403306560
115709546157095462GA10GENIChomozygous138997462
115709546157095462G10GENICheterozygous403306561
115709547057095471GA13GENIChomozygous138997463
115709547057095471G13GENICheterozygous403306562
115709555257095553GA1GENIChomozygous138997464
115721514157215142TC18GENICpossibly homozygous138997465
115719218657192187GA47GENIChomozygous144427410
115716514057165142AC27GENICheterozygous144421285
115718413157184132A36GENICheterozygous138890609
115727493157274933CA14GENICheterozygous144421286
115730971957309720C28GENICheterozygous403641303
115730971957309720CG28GENICpossibly homozygous403641304
115754075057540751CT22GENIChomozygous144427411
115757636257576363A29GENIChomozygous403306567
115757636257576363AG29GENICheterozygous403306568
115760386257603863T11GENICheterozygous403306583
115760386257603863TA11GENICheterozygous403306584
115760622957606230A47GENICpossibly homozygous138890612
115765577557655776GA38GENIChomozygous144427412
115769505957695060GT15GENICheterozygous144427413
115773207657732077GT20GENICpossibly homozygous404916303