chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 108396766 108396767 T C 43 GENIC homozygous 51596096 10 108397090 108397091 G T 8 GENIC homozygous 51596098 10 108397871 108397872 C T 43 GENIC homozygous 51596100 10 108398368 108398369 A G 41 GENIC homozygous 51596104 10 108398863 108398864 T C 38 GENIC homozygous 51596106 10 108399592 108399593 C T 21 GENIC homozygous 51596108 10 108400014 108400015 C CTCT 48 GENIC heterozygous 51953766 10 108400020 108400021 T C 55 GENIC heterozygous 51953769 10 108400449 108400450 A G 30 GENIC homozygous 51596112 10 108401441 108401449 GTGTGTGT -------- 4 GENIC heterozygous 51596114 10 108401486 108401487 T C 19 GENIC homozygous 51596116 10 108402283 108402284 A G 30 GENIC homozygous 51596118 10 108403550 108403551 T TAAC 15 GENIC homozygous 51596120 10 108403553 108403554 G GGGCTAC 10 GENIC homozygous 51596122 10 108403922 108403924 AA -- 20 GENIC homozygous 51596124 10 108405663 108405664 T TC 26 GENIC homozygous 51596126 10 108407879 108407880 A T 38 GENIC homozygous 51596132 10 108408887 108408888 T TC 10 GENIC homozygous 51596134 10 108409221 108409222 T TCA 7 GENIC heterozygous 51596138 10 108409485 108409486 A G 19 GENIC homozygous 51596140 10 108410258 108410259 T A 33 GENIC homozygous 51596142 10 108411935 108411936 C T 28 GENIC heterozygous 51596146 10 108412065 108412066 G A 26 GENIC homozygous 51596148 10 108412067 108412068 C CT 28 GENIC homozygous 51596149 10 108401484 108401485 T C 19 GENIC homozygous 52271543 10 108402257 108402258 C T 26 GENIC homozygous 52271545 10 108402268 108402269 A T 25 GENIC homozygous 52271547 10 108403116 108403117 A G 41 GENIC homozygous 52271549 10 108406307 108406308 C T 35 GENIC homozygous 52271551 10 108407071 108407072 T G 9 GENIC heterozygous 52271553 10 108407075 108407076 T G 9 GENIC heterozygous 52271555 10 108406936 108406944 GTGTGTGT -------- 4 GENIC homozygous 52216626 10 108412524 108412525 C T 28 GENIC homozygous 51596151 10 108412774 108412775 T C 33 GENIC homozygous 51596153