chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157613725157613726GA35GENIChomozygous112906742
4157613853157613854GT30GENIChomozygous112906744
4157614185157614186TG29GENIChomozygous112906746
4157614774157614775AT32GENIChomozygous112906748
4157616535157616536CA18GENIChomozygous112906752
4157619978157619979GT28GENIChomozygous112906754
4157620744157620745TC28GENIChomozygous112906756
4157621147157621148CT14GENIChomozygous112906758
4157623083157623084GA29GENIChomozygous112906760
4157625710157625711CT30GENIChomozygous112906762
4157626447157626448TC27GENIChomozygous112906764
4157627043157627044TC34GENIChomozygous112906766
4157629525157629526TC24GENIChomozygous112906768
4157630918157630919GT8GENIChomozygous112906770
4157631950157631951AG39GENIChomozygous112906772
4157632657157632658TC22GENIChomozygous112906774
4157633500157633501AG24GENIChomozygous112906776
4157634098157634099TC29GENIChomozygous112906778
4157635239157635240AC14GENIChomozygous112906780
4157635295157635296CT19GENIChomozygous112906782
4157638495157638496TC21GENIChomozygous112906784
4157639657157639658GC28GENIChomozygous112906786
4157644216157644217CG45GENIChomozygous112906788
4157644340157644341TC37GENIChomozygous112906790