chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 145361900 145361901 G C 12 GENIC homozygous 631120560 5 145363113 145363114 A - 3 GENIC homozygous 745550902 5 145363698 145363699 G GAC 12 GENIC homozygous 745550903 5 145364001 145364002 C T 27 GENIC possibly homozygous 631120561 5 145364976 145364977 A G 19 GENIC possibly homozygous 631120562 5 145365273 145365274 C CAGTT 7 GENIC homozygous 745550904 5 145365364 145365365 T C 25 GENIC homozygous 631120563 5 145365509 145365510 C T 17 GENIC homozygous 631120564 5 145367107 145367108 C T 19 GENIC homozygous 631120565 5 145367301 145367302 T G 18 GENIC possibly homozygous 631120566 5 145367841 145367842 A C 19 GENIC homozygous 631120567 5 145367882 145367883 T G 6 GENIC homozygous 631120568 5 145367888 145367889 C T 6 GENIC homozygous 631120569 5 145369147 145369148 T C 23 GENIC possibly homozygous 631120570 5 145370313 145370314 A - 1 GENIC homozygous 745550905 5 145370535 145370536 G A 20 GENIC possibly homozygous 631120571 5 145370676 145370677 A AAAAC 5 GENIC homozygous 745550907 5 145371166 145371167 G T 5 GENIC homozygous 631120572 5 145371167 145371168 T C 4 GENIC homozygous 631120573 5 145373159 145373160 T C 14 GENIC possibly homozygous 631120574 5 145373253 145373254 T G 11 GENIC homozygous 631120575 5 145373669 145373670 C T 20 GENIC homozygous 631120576 5 145378991 145378992 T TC 2 GENIC homozygous 745550908