chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157613725157613726GA35GENIChomozygous112906742
4157613853157613854GT26GENIChomozygous112906744
4157614185157614186TG30GENIChomozygous112906746
4157614774157614775AT32GENIChomozygous112906748
4157614977157614978AC23GENIChomozygous112906750
4157616535157616536CA20GENIChomozygous112906752
4157619978157619979GT15GENIChomozygous112906754
4157620744157620745TC23GENIChomozygous112906756
4157621147157621148CT20GENIChomozygous112906758
4157623083157623084GA34GENIChomozygous112906760
4157625710157625711CT16GENIChomozygous112906762
4157626447157626448TC21GENIChomozygous112906764
4157627043157627044TC24GENIChomozygous112906766
4157629525157629526TC18GENIChomozygous112906768
4157630918157630919GT19GENIChomozygous112906770
4157631950157631951AG25GENIChomozygous112906772
4157632657157632658TC29GENIChomozygous112906774
4157633500157633501AG32GENIChomozygous112906776
4157634098157634099TC24GENIChomozygous112906778
4157635239157635240AC22GENIChomozygous112906780
4157635295157635296CT24GENIChomozygous112906782
4157638495157638496TC18GENIChomozygous112906784
4157639366157639366C14GENIChomozygous128096215
4157628913157628913GT25GENIChomozygous128096211
4157633855157633859TGTC29GENIChomozygous128096212
4157637454157637460CCCCTG16GENIChomozygous128096213
4157637690157637708CAGGAGGGAGGGTGCAGC27GENIChomozygous128096214
4157639657157639658GC17GENIChomozygous112906786
4157644340157644341TC23GENIChomozygous112906790
4157644216157644217CG26GENIChomozygous112906788