chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123122120123122121AG36GENICpossibly homozygous54089071
7123123207123123208AG40GENIChomozygous54089072
7123123324123123325CT24GENIChomozygous54089073
7123123347123123348TC26GENIChomozygous54089074
7123125166123125167GA33GENIChomozygous54089075
7123126122123126124GG--1GENIChomozygous54089076
7123126507123126512CCAGG-----24GENIChomozygous54089077
7123127024123127025CT52GENIChomozygous54089078
7123127049123127050CT40GENIChomozygous54089079
7123127124123127125GA38GENIChomozygous54089080
7123127749123127750GA57GENICheterozygous54089081
7123128600123128601AG32GENIChomozygous54089082
7123128766123128767TC36GENIChomozygous54089083
7123128823123128824TC55GENIChomozygous54089084
7123129185123129186CT34GENIChomozygous54089085
7123129452123129453AG45GENIChomozygous54089086
7123129887123129888AG25GENIChomozygous54089087
7123129922123129933ACAGCACTAGA-----------13GENIChomozygous54089088
7123130199123130200TC37GENIChomozygous54089089
7123130410123130411G-35GENIChomozygous54235796
7123130783123130784TG18GENIChomozygous54089090
7123131026123131027TG34GENICpossibly homozygous54089091
7123131082123131084GG--25GENICheterozygous54089092
7123131084123131086TT--12GENICheterozygous54089093
7123131108123131109GA21GENIChomozygous54089094
7123131483123131484GA40GENIChomozygous54089095