chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121492291114922912AT18GENIChomozygous50069974
121492557614925577CT27GENICpossibly homozygous50069976
121492559614925597CCAT26GENICpossibly homozygous50069978
121492892214928923CT17GENIChomozygous50069980
121493079314930803GTACCAGACG----------23GENIChomozygous50069988
121493620814936248GACGGCCTCTGCATCCCACTGACGGCCTCTGCATCCCACT----------------------------------------18GENICpossibly homozygous50533337
121493892314938924CT33GENIChomozygous50069994
121493995214939962CACACACACA----------12GENICheterozygous50533339
121493995414939962CACACACA--------12GENICheterozygous50533341
121494306614943067TTGTGTGTGTGTGC4GENIChomozygous50533343
121494333614943337AG23GENIChomozygous50069998
121494513014945131CT39GENIChomozygous50070000
121494554514945546GA44GENIChomozygous50070002
121494581314945814CA26GENIChomozygous50070004
121494590214945903GA35GENIChomozygous50070006
121494591214945913CT34GENIChomozygous50070008
121494646214946463TG26GENIChomozygous50070010
121495143314951434AG23GENIChomozygous50070012
121495147114951472CT26GENIChomozygous50070014