chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 95386608 95386609 T C 39 GENIC homozygous 68186957 10 95386711 95386712 A G 29 GENIC homozygous 68186961 10 95386752 95386753 A T 26 GENIC homozygous 68186964 10 95387091 95387092 C T 35 GENIC possibly homozygous 68471394 10 95387143 95387144 A G 44 GENIC possibly homozygous 68186967 10 95387349 95387350 G A 58 GENIC homozygous 68471397 10 95387836 95387837 C G 60 GENIC homozygous 68186971 10 95388095 95388096 G A 61 GENIC homozygous 68186974 10 95388524 95388525 A G 22 GENIC homozygous 68186978 10 95389225 95389226 G A 51 GENIC possibly homozygous 68186986 10 95391345 95391346 C T 30 GENIC possibly homozygous 68187053 10 95391438 95391439 G A 18 GENIC heterozygous 68187057 10 95391741 95391742 C T 49 GENIC possibly homozygous 68471403 10 95391846 95391847 C T 59 GENIC homozygous 68187065 10 95392045 95392046 C G 14 GENIC possibly homozygous 68471406 10 95392635 95392636 T C 67 GENIC homozygous 68471410 10 95394170 95394171 G A 54 GENIC possibly homozygous 68471414 10 95394506 95394507 G A 50 GENIC homozygous 68471417 10 95394933 95394934 T C 34 GENIC homozygous 68187096 10 95395190 95395191 T C 51 GENIC possibly homozygous 68471420 10 95395351 95395352 C T 62 GENIC homozygous 68471423 10 95396838 95396839 C G 12 GENIC heterozygous 68187112 10 95396839 95396840 G T 12 GENIC heterozygous 68471426 10 95397373 95397374 C T 55 GENIC homozygous 68471428 10 95398082 95398083 A G 54 GENIC possibly homozygous 68471432 10 95398099 95398100 C T 47 GENIC possibly homozygous 68471435 10 95398264 95398265 A G 48 GENIC homozygous 68471438 10 95398569 95398570 T C 44 GENIC homozygous 68187119 10 95398645 95398646 C T 32 GENIC homozygous 68471440 10 95399339 95399340 G A 83 GENIC homozygous 68471443 10 95391388 95391389 A G 13 GENIC heterozygous 68673133 10 95397074 95397075 T G 50 GENIC heterozygous 68673135