chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2257398404257398405CG39GENIChomozygous110411893
2257399081257399082A37GENICpossibly homozygous127768530
2257399108257399109AT38GENIChomozygous120385072
2257399519257399520CT29GENIChomozygous131323495
2257399708257399710TG2GENIChomozygous132569181
2257400269257400270CT5GENIChomozygous131323496
2257403118257403119T44GENIChomozygous127768532
2257403328257403329TC55GENIChomozygous121725018
2257403607257403608AG43GENIChomozygous110411899
2257407718257407719CT68GENIChomozygous110411909
2257407770257407771GA62GENICpossibly homozygous111043658
2257411587257411588GA47GENIChomozygous120385073
2257414364257414365AC37GENIChomozygous120385074
2257414365257414366AC37GENIChomozygous110411919
2257415716257415717TC56GENIChomozygous110411923
2257416869257416870TG56GENIChomozygous110411929
2257416898257416899TG62GENIChomozygous120385075
2257417045257417046CT40GENIChomozygous120385076
2257419578257419579TC84GENICheterozygous110411935
2257419882257419882A74GENICheterozygous133381115
2257419989257419990GA73GENICheterozygous110411937
2257420036257420037GA73GENICheterozygous110411939
2257420137257420139AG66GENICheterozygous127768534
2257424826257424827TC42GENIChomozygous120385077
2257425220257425221CT40GENIChomozygous120385078
2257408244257408276GTACCAGGCAGTCGCTTAGGATCTAGCCTGCC38GENIChomozygous131304651
2257408329257408365TCTAGCCTGCCGTAGCGTGCAGTCAGTCGCTCAGGA29GENIChomozygous131304652