chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 143066632 143066633 A G 50 GENIC homozygous 533107830 4 143067173 143067174 T A 40 GENIC homozygous 533107831 4 143067462 143067463 A G 70 GENIC homozygous 533107832 4 143067524 143067525 C T 71 GENIC homozygous 533107833 4 143067604 143067605 C T 58 GENIC homozygous 533107834 4 143068021 143068022 A G 72 GENIC homozygous 533107835 4 143068398 143068399 C T 55 GENIC possibly homozygous 533107836 4 143068696 143068697 A G 48 GENIC homozygous 533107837 4 143068742 143068743 A G 59 GENIC homozygous 533107838 4 143068861 143068862 A G 56 GENIC homozygous 533107839 4 143068953 143068954 G A 41 GENIC homozygous 533107840 4 143068972 143068975 TTT --- 28 GENIC homozygous 695497488 4 143069008 143069009 G A 31 GENIC homozygous 533107841 4 143069122 143069123 G A 46 GENIC homozygous 533107842 4 143069164 143069165 C T 44 GENIC homozygous 533107843 4 143069280 143069281 C T 49 GENIC homozygous 533107844 4 143069285 143069286 G T 48 GENIC homozygous 533107845 4 143069345 143069346 G A 66 GENIC homozygous 533107846 4 143069379 143069380 G C 55 GENIC homozygous 533107847 4 143069523 143069524 A C 50 GENIC homozygous 533107848 4 143071303 143071304 G T 31 GENIC homozygous 533107849 4 143071742 143071743 A C 54 GENIC homozygous 533107850 4 143072361 143072362 C T 36 GENIC possibly homozygous 536556656 4 143072689 143072690 G A 50 GENIC possibly homozygous 533107851 4 143072830 143072831 T G 53 GENIC heterozygous 536556657