chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 56081946 56081947 T C 43 GENIC homozygous 110361039 18 56084396 56084397 G A 59 GENIC possibly homozygous 119495630 18 56085085 56085086 G A 55 GENIC homozygous 119495631 18 56088398 56088399 C T 47 GENIC homozygous 110361041 18 56089193 56089194 A G 57 GENIC homozygous 110361043 18 56090158 56090159 T C 43 GENIC homozygous 110361045 18 56090937 56090938 G A 45 GENIC homozygous 110361047 18 56091568 56091569 C T 48 GENIC homozygous 110361049 18 56091796 56091797 T C 49 GENIC homozygous 110361051 18 56092776 56092777 C T 50 GENIC possibly homozygous 110361053 18 56093180 56093181 T C 44 GENIC homozygous 110361055 18 56094514 56094515 C A 53 GENIC homozygous 110361057 18 56094672 56094673 A G 25 GENIC homozygous 110361060 18 56094848 56094849 T C 48 GENIC homozygous 110361062 18 56096620 56096621 C T 41 GENIC homozygous 110361064 18 56096907 56096908 T C 49 GENIC homozygous 110361066 18 56097468 56097469 A G 55 GENIC homozygous 110361068 18 56098437 56098438 A G 47 GENIC homozygous 110361070 18 56099321 56099322 G T 48 GENIC homozygous 110361072 18 56099522 56099523 G A 39 GENIC homozygous 110361074 18 56100114 56100115 G T 47 GENIC possibly homozygous 119495632 18 56100174 56100175 G T 45 GENIC heterozygous 119495633 18 56103238 56103239 G A 46 GENIC homozygous 110361076 18 56103328 56103329 G A 44 GENIC homozygous 110361078 18 56103736 56103737 A G 40 GENIC possibly homozygous 110655387 18 56104191 56104192 A G 40 GENIC homozygous 110361080 18 56105722 56105723 A G 64 GENIC homozygous 110361082 18 56106473 56106474 T C 40 GENIC homozygous 110361084 18 56107117 56107118 C T 44 GENIC homozygous 110361086 18 56108584 56108585 T C 45 GENIC homozygous 110361088 18 56109136 56109137 G A 35 GENIC homozygous 110361090 18 56110961 56110962 T G 45 GENIC possibly homozygous 110361092 18 56112689 56112690 A C 52 GENIC homozygous 110361094 18 56113181 56113182 A G 47 GENIC homozygous 110361096