chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31538020615380207CG22GENIChomozygous120077239
31538105215381053CT15GENICpossibly homozygous119775168
31538156715381568AC23GENIChomozygous119775170
31538413615384137TG32GENIChomozygous111881545
31538511615385117AG20GENIChomozygous111454646
31538794515387946CT11GENIChomozygous119775174
31538801615388017CG33GENICpossibly homozygous120077240
31539025715390258GA14GENIChomozygous119775176
31539027615390277GA22GENIChomozygous120077241
31539057415390575GA29GENICpossibly homozygous119775178
31539195815391959TC20GENIChomozygous111881567
31539281915392820CT23GENICpossibly homozygous120077242
31539857715398578TC29GENIChomozygous111881577
31539909015399091TC14GENIChomozygous111881579
31539952715399528TC12GENIChomozygous111454649
31540091215400913GA26GENICpossibly homozygous120077243
31540174215401743CT38GENIChomozygous111881591
31540183215401833TG31GENIChomozygous111454652
31540363915403640GC21GENIChomozygous111881593
31540364415403645GT17GENIChomozygous111881595
31540466615404667GA11GENIChomozygous111454655
31540657115406572AG25GENIChomozygous111454656
31540664915406650CG29GENIChomozygous111454657