chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 72146374 72146375 T - 41 GENIC homozygous 759976138 18 72146422 72146423 T - 28 GENIC homozygous 759976139 18 72147716 72147717 A G 36 GENIC possibly homozygous 654877197 18 72148733 72148736 GGG --- 6 GENIC heterozygous 759976140 18 72148734 72148736 GG -- 6 GENIC heterozygous 759976141 18 72156410 72156411 T C 30 GENIC homozygous 654877198 18 72157694 72157695 G A 30 GENIC homozygous 654877199 18 72160045 72160046 A G 34 GENIC homozygous 654877200 18 72160657 72160659 AA -- 25 GENIC homozygous 759976143 18 72160953 72160957 TGTG ---- 10 GENIC heterozygous 759976144 18 72160955 72160957 TG -- 10 GENIC heterozygous 759976145 18 72161766 72161767 A ACATGCACACAGAACACATG 17 GENIC homozygous 759976149 18 72162728 72162729 G A 19 GENIC homozygous 654877201 18 72165697 72165698 A G 28 GENIC possibly homozygous 654877202 18 72166951 72166952 A C 24 GENIC homozygous 654877203 18 72167270 72167271 A G 33 GENIC homozygous 654877204 18 72167484 72167485 A G 43 GENIC homozygous 654877205 18 72167493 72167494 G A 40 GENIC homozygous 654877206 18 72168470 72168471 G A 31 GENIC homozygous 654877207 18 72168488 72168489 T C 34 GENIC homozygous 654877208 18 72168617 72168618 G A 28 GENIC homozygous 654877209 18 72168744 72168745 G C 27 GENIC homozygous 654877210