chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 108396766 108396767 T C 18 GENIC homozygous 51596096 10 108397090 108397091 G T 25 GENIC homozygous 51596098 10 108397871 108397872 C T 17 GENIC homozygous 51596100 10 108397987 108397988 C T 14 GENIC heterozygous 51596102 10 108398368 108398369 A G 12 GENIC homozygous 51596104 10 108398613 108398614 C T 14 GENIC heterozygous 53547848 10 108398863 108398864 T C 17 GENIC homozygous 51596106 10 108399592 108399593 C T 16 GENIC homozygous 51596108 10 108400449 108400450 A G 15 GENIC homozygous 51596112 10 108401486 108401487 T C 10 GENIC homozygous 51596116 10 108402283 108402284 A G 13 GENIC homozygous 51596118 10 108403922 108403924 AA -- 17 GENIC homozygous 51596124 10 108405663 108405664 T TC 16 GENIC homozygous 51596126 10 108406307 108406308 C T 19 GENIC heterozygous 52271551 10 108401484 108401485 T C 10 GENIC heterozygous 52271543 10 108402257 108402258 C T 17 GENIC heterozygous 52271545 10 108402268 108402269 A T 13 GENIC heterozygous 52271547 10 108403116 108403117 A G 13 GENIC heterozygous 52271549 10 108407879 108407880 A T 13 GENIC homozygous 51596132 10 108408876 108408877 A T 9 GENIC homozygous 52409531 10 108409221 108409222 T TC 11 GENIC heterozygous 53547849 10 108409222 108409223 A C 11 GENIC heterozygous 52409533 10 108409485 108409486 A G 11 GENIC homozygous 51596140 10 108410258 108410259 T A 14 GENIC homozygous 51596142 10 108410992 108410993 C T 15 GENIC heterozygous 51772052 10 108411935 108411936 C T 12 GENIC heterozygous 51596146 10 108412065 108412066 G A 22 GENIC homozygous 51596148 10 108412067 108412068 C CT 22 GENIC homozygous 51596149 10 108412524 108412525 C T 18 GENIC homozygous 51596151 10 108412774 108412775 T C 10 GENIC homozygous 51596153 10 108411934 108411935 A ATGCG 12 GENIC heterozygous 53561834