chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3134684987134684990TTT---8GENIChomozygous57689004
3134684993134684994TG8GENIChomozygous57689005
3134685303134685304AG64GENIChomozygous57689006
3134685875134685876AG57GENIChomozygous57689007
3134686227134686228CT60GENIChomozygous57689008
3134686230134686231AG60GENIChomozygous57689009
3134686248134686249AG55GENIChomozygous57689010
3134686614134686615CT96GENIChomozygous57689011
3134686905134686906T-4GENIChomozygous57689012
3134688862134688863CT68GENIChomozygous57689013
3134688972134688973GT61GENIChomozygous57689014
3134689084134689085GT48GENIChomozygous57689015
3134689145134689146TTTTTG50GENIChomozygous57689016
3134690546134690547G-40GENIChomozygous57689017
3134692735134692736TC41GENIChomozygous57689019
3134692804134692807CTT---25GENIChomozygous57689020
3134694058134694061CTT---68GENIChomozygous57689021
3134694943134694944GA79GENICpossibly homozygous57689022