chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13103397346103397347GC29GENIChomozygous114438013
13103397351103397352CA29GENICpossibly homozygous114438015
13103397371103397372CT32GENIChomozygous114438017
13103397644103397645CA18GENIChomozygous118467719
13103397645103397646CG18GENIChomozygous118467720
13103397646103397647CG18GENIChomozygous118467721
13103397647103397648CG18GENIChomozygous118467722
13103397651103397652CA19GENIChomozygous114438019
13103399418103399419TG38GENIChomozygous118551056
13103399438103399439CT36GENIChomozygous118467724
13103399475103399476CT24GENIChomozygous118467725
13103399544103399545AC22GENIChomozygous118467726
13103400747103400748GT32GENIChomozygous114438021
13103400886103400887TG35GENIChomozygous114588834
13103400963103400964CT8GENIChomozygous118467727
13103401272103401273AG41GENIChomozygous114438027
13103401273103401274GA42GENIChomozygous115018532
13103401292103401293CA34GENIChomozygous115018534
13103401418103401419TA48GENIChomozygous114725661
13103402508103402509TC44GENICheterozygous118551057
13103402628103402629CT45GENICheterozygous118467728
13103402667103402668CT17GENICheterozygous118467729
13103402670103402671CT14GENICheterozygous118551058
13103402676103402677CT8GENIChomozygous118467730
13103402751103402752AT8GENIChomozygous118467732
13103402763103402764CT11GENIChomozygous118467733