chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 121351511 121351512 A C 24 GENIC homozygous 941421695 7 121351659 121351660 A G 19 GENIC homozygous 941421696 7 121351666 121351667 G A 19 GENIC homozygous 941421697 7 121352112 121352113 A G 26 GENIC homozygous 941421698 7 121352821 121352822 A G 23 GENIC homozygous 941421699 7 121353851 121353852 A T 19 GENIC homozygous 941421700 7 121357005 121357006 T G 40 GENIC homozygous 941421701 7 121357109 121357110 G A 22 GENIC homozygous 941421702 7 121357662 121357663 C T 30 GENIC homozygous 941421703 7 121366941 121366942 A T 6 GENIC homozygous 941421704 7 121370431 121370432 T C 33 GENIC homozygous 941421705 7 121370670 121370671 G A 20 GENIC homozygous 941421706 7 121372869 121372870 T C 28 GENIC homozygous 941421707 7 121374131 121374132 A G 43 GENIC homozygous 941421708 7 121376034 121376035 G A 37 GENIC homozygous 941421709 7 121376233 121376234 T C 22 GENIC homozygous 941421710 7 121377012 121377013 G A 26 GENIC homozygous 941421711 7 121377413 121377414 A G 25 GENIC homozygous 941421712 7 121378332 121378333 T C 28 GENIC homozygous 941421713 7 121378486 121378487 G A 39 GENIC homozygous 941421714 7 121378756 121378757 T C 28 GENIC homozygous 941421715 7 121380634 121380635 T C 41 GENIC homozygous 941421716 7 121381943 121381944 T C 46 GENIC homozygous 941421717