chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 108396355 108396371 GTGTGTGTGTGTGTGT ---------------- 5 GENIC heterozygous 51596094 10 108396766 108396767 T C 44 GENIC homozygous 51596096 10 108397090 108397091 G T 68 GENIC homozygous 51596098 10 108397871 108397872 C T 40 GENIC homozygous 51596100 10 108397987 108397988 C T 62 GENIC possibly homozygous 51596102 10 108398368 108398369 A G 31 GENIC homozygous 51596104 10 108398863 108398864 T C 48 GENIC homozygous 51596106 10 108399592 108399593 C T 72 GENIC homozygous 51596108 10 108400021 108400024 TCC --- 33 GENIC homozygous 51596110 10 108400449 108400450 A G 62 GENIC homozygous 51596112 10 108401441 108401449 GTGTGTGT -------- 5 GENIC homozygous 51596114 10 108401486 108401487 T C 30 GENIC possibly homozygous 51596116 10 108402283 108402284 A G 46 GENIC homozygous 51596118 10 108403550 108403551 T TAAC 17 GENIC homozygous 51596120 10 108403553 108403554 G GGGCTAC 7 GENIC homozygous 51596122 10 108403922 108403924 AA -- 60 GENIC homozygous 51596124 10 108405663 108405664 T TC 57 GENIC homozygous 51596126 10 108407055 108407057 TT -- 21 GENIC homozygous 51596130 10 108401478 108401479 T C 27 GENIC heterozygous 51772050 10 108407879 108407880 A T 60 GENIC homozygous 51596132 10 108408887 108408888 T TC 27 GENIC heterozygous 51596134 10 108408887 108408888 T TTC 27 GENIC heterozygous 51596136 10 108409221 108409222 T TCA 59 GENIC homozygous 51596138 10 108409485 108409486 A G 63 GENIC homozygous 51596140 10 108410258 108410259 T A 47 GENIC possibly homozygous 51596142 10 108410992 108410993 C T 67 GENIC homozygous 51772052 10 108411935 108411936 C T 32 GENIC heterozygous 51596146 10 108412065 108412066 G A 51 GENIC homozygous 51596148 10 108412067 108412068 C CT 55 GENIC homozygous 51596149 10 108412225 108412226 C T 57 GENIC homozygous 51772054 10 108412524 108412525 C T 67 GENIC homozygous 51596151 10 108412774 108412775 T C 57 GENIC homozygous 51596153