chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 230368917 230368919 TG -- 9 GENIC homozygous 59431827 2 230368962 230368963 T TTGTGTGTGTGTGTG 11 GENIC homozygous 60520636 2 230370303 230370304 T TTC 17 GENIC possibly homozygous 59431828 2 230370879 230370880 C T 17 GENIC homozygous 59431830 2 230376793 230376794 G A 35 GENIC homozygous 59431831 2 230379604 230379605 T TTCATCATCATCATCA 12 GENIC homozygous 60594492 2 230379740 230379741 C CAAAAAAAAAAAAA 13 GENIC homozygous 60458944 2 230380529 230380530 C T 33 GENIC homozygous 59431834 2 230383135 230383136 T C 36 GENIC possibly homozygous 59431835 2 230383623 230383627 AAAT ---- 2 GENIC homozygous 59431836 2 230384350 230384351 C G 42 GENIC homozygous 59431837 2 230386113 230386114 C CTTTTTTTTTT 13 GENIC heterozygous 60520637 2 230389865 230389866 T TACACAC 17 GENIC heterozygous 60550455 2 230389866 230389868 AC -- 17 GENIC possibly homozygous 60550456 2 230391218 230391219 C T 27 GENIC homozygous 59431842 2 230393014 230393015 G - 34 GENIC possibly homozygous 59431843 2 230394024 230394025 A G 36 GENIC possibly homozygous 59431844 2 230394444 230394445 T C 48 GENIC homozygous 59431845 2 230394477 230394478 T C 49 GENIC homozygous 59431846 2 230394866 230394867 C CA 27 GENIC homozygous 59431847 2 230395033 230395034 A - 12 GENIC heterozygous 60594494 2 230395393 230395394 G A 42 GENIC homozygous 59431848 2 230398591 230398592 A G 34 GENIC homozygous 59431849