chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41541094915410953ATAT----16GENICheterozygous56763838
41541095115410953AT--16GENICpossibly homozygous58722984
41541491715414919AC--3GENICheterozygous56763846
41541584615415847AAT23GENIChomozygous57428544
41541821015418211TTACAC3GENIChomozygous56763852
41542041115420412GGGTGT2GENIChomozygous57428548
41542295115422953GT--7GENIChomozygous57428550
41542433215424333C-21GENIChomozygous56763862
41543243115432432AAATAT6GENIChomozygous58722986
41544726515447266A-12GENIChomozygous57428554
41545142715451428CCGT1GENIChomozygous58523501
41545185615451857CCA19GENIChomozygous56763915
41545322215453223TC24GENICheterozygous56763918
41545324515453246GT21GENICheterozygous56763919
41546802015468022TG--3GENICheterozygous58328277
41542924815429252GATA----10GENIChomozygous58328273
41544616115446163GA--9GENICheterozygous58328274
41545100615451007CCGT3GENIChomozygous58328275
41546185015461852TC--3GENIChomozygous58328276
41547122115471222A-19GENIChomozygous57428556
41547125215471261TAATAATAA---------9GENIChomozygous56763947
41547210515472106G-23GENIChomozygous57428558
41547245415472455TTAA19GENIChomozygous57428560
41547263015472631AG23GENIChomozygous57428562
41547350215473503GA20GENIChomozygous56763949
41547404915474050CT19GENIChomozygous57428564
41547411315474114TC13GENIChomozygous57428566
41547526115475262C-22GENIChomozygous57428568
41547579615475797AG27GENIChomozygous57428570
41547601815476019C-22GENIChomozygous57428572
41547631715476318TC10GENIChomozygous57428574
41547644315476444AG15GENIChomozygous57428576
41547676715476768CCA23GENIChomozygous57428578
41547711215477113TC33GENICpossibly homozygous57428580
41547874815478749AACC6GENIChomozygous57265651