chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 56010732 56010733 T C 48 GENIC homozygous 930856120 19 56011013 56011014 C T 38 GENIC possibly homozygous 930856121 19 56011203 56011204 C T 31 GENIC homozygous 930856122 19 56011979 56011980 C T 46 GENIC homozygous 930856123 19 56012029 56012030 G A 43 GENIC homozygous 930856124 19 56012468 56012469 C A 61 GENIC homozygous 930856125 19 56012835 56012836 T C 37 GENIC homozygous 930856126 19 56014649 56014650 C G 37 GENIC homozygous 930856127 19 56014664 56014665 A G 38 GENIC homozygous 930856128 19 56014888 56014889 A T 42 GENIC homozygous 930856129 19 56016113 56016114 C A 58 GENIC homozygous 930856130 19 56016888 56016889 G A 39 GENIC homozygous 930856131 19 56017375 56017376 C T 26 GENIC homozygous 930856132 19 56017436 56017437 T A 31 GENIC homozygous 930856133 19 56017905 56017906 T C 35 GENIC homozygous 930856134 19 56018570 56018571 G A 66 GENIC homozygous 930856135 19 56019292 56019293 T C 37 GENIC homozygous 930856136 19 56019695 56019696 C T 36 GENIC homozygous 930856137 19 56019753 56019754 A G 32 GENIC homozygous 930856138 19 56019944 56019945 C T 33 GENIC homozygous 930856139 19 56020331 56020332 G A 47 GENIC homozygous 930856140 19 56020497 56020498 T C 54 GENIC homozygous 930856141 19 56021385 56021386 C A 31 GENIC homozygous 930856142