chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 108396766 108396767 T C 9 GENIC homozygous 51596096 10 108397090 108397091 G T 21 GENIC homozygous 51596098 10 108397871 108397872 C T 16 GENIC homozygous 51596100 10 108398368 108398369 A G 12 GENIC homozygous 51596104 10 108398863 108398864 T C 16 GENIC homozygous 51596106 10 108399592 108399593 C T 14 GENIC homozygous 51596108 10 108400449 108400450 A G 17 GENIC homozygous 51596112 10 108401486 108401487 T C 6 GENIC homozygous 51596116 10 108402283 108402284 A G 14 GENIC homozygous 51596118 10 108403922 108403924 AA -- 20 GENIC homozygous 51596124 10 108405663 108405664 T TC 18 GENIC homozygous 51596126 10 108407879 108407880 A T 14 GENIC homozygous 51596132 10 108408876 108408877 A T 11 GENIC homozygous 52409531 10 108408887 108408888 T C 11 GENIC homozygous 51953781 10 108409485 108409486 A G 19 GENIC homozygous 51596140 10 108410258 108410259 T A 16 GENIC homozygous 51596142 10 108411935 108411936 C T 11 GENIC homozygous 51596146 10 108412065 108412066 G A 11 GENIC homozygous 51596148 10 108412067 108412068 C CT 11 GENIC homozygous 51596149 10 108402257 108402258 C T 19 GENIC homozygous 52271545 10 108402268 108402269 A T 15 GENIC homozygous 52271547 10 108403116 108403117 A G 11 GENIC homozygous 52271549 10 108406307 108406308 C T 18 GENIC homozygous 52271551 10 108406576 108406577 A - 8 GENIC heterozygous 53533266 10 108412524 108412525 C T 24 GENIC homozygous 51596151 10 108412774 108412775 T C 23 GENIC homozygous 51596153