chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121492291114922912AT23GENIChomozygous50069974
121492556414925566CG--5GENICheterozygous50568158
121492557614925577CT19GENICpossibly homozygous50069976
121492559614925597CCAT15GENIChomozygous50069978
121492892214928923CT16GENIChomozygous50069980
121493079314930803GTACCAGACG----------21GENIChomozygous50069988
121493620814936248GACGGCCTCTGCATCCCACTGACGGCCTCTGCATCCCACT----------------------------------------3GENIChomozygous50533337
121493892314938924CT22GENIChomozygous50069994
121493995214939962CACACACACA----------11GENICheterozygous50533339
121493995414939962CACACACA--------11GENICheterozygous50533341
121494306614943067TTGTGTGTGTGTGTGTGC2GENICheterozygous50560547
121494306614943067TTGTGTGTGTGTGC2GENICheterozygous50533343
121494333614943337AG26GENIChomozygous50069998
121494513014945131CT23GENIChomozygous50070000
121494554514945546GA15GENIChomozygous50070002
121494581314945814CA21GENIChomozygous50070004
121494590214945903GA28GENIChomozygous50070006
121494591214945913CT30GENIChomozygous50070008
121494646214946463TG34GENIChomozygous50070010
121495143314951434AG16GENIChomozygous50070012
121495147114951472CT21GENIChomozygous50070014