chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 230368917 230368919 TG -- 6 GENIC homozygous 753425961 2 230368962 230368963 T TTGTGTGTGTGTGTG 3 GENIC heterozygous 753425962 2 230370303 230370304 T TTC 11 GENIC heterozygous 753425963 2 230370879 230370880 C T 24 GENIC homozygous 643896242 2 230376793 230376794 G A 25 GENIC homozygous 643896243 2 230379604 230379605 T TTCATCATCA 9 GENIC homozygous 753425965 2 230379740 230379741 C CAAAAAAAAAAAAA 11 GENIC homozygous 753425968 2 230380529 230380530 C T 28 GENIC homozygous 643896244 2 230383135 230383136 T C 22 GENIC homozygous 643896245 2 230383623 230383627 AAAT ---- 9 GENIC homozygous 753425969 2 230384350 230384351 C G 20 GENIC homozygous 643896246 2 230386113 230386114 C CTTTTTTTTTT 4 GENIC homozygous 753425970 2 230389865 230389866 T TACACAC 11 GENIC heterozygous 753425973 2 230389866 230389868 AC -- 11 GENIC possibly homozygous 753425971 2 230391218 230391219 C T 29 GENIC homozygous 643896247 2 230393014 230393015 G - 13 GENIC homozygous 753425974 2 230394024 230394025 A G 24 GENIC homozygous 643896248 2 230394444 230394445 T C 18 GENIC homozygous 643896249 2 230394477 230394478 T C 25 GENIC homozygous 643896250 2 230394866 230394867 C CA 18 GENIC homozygous 753425977 2 230395393 230395394 G A 28 GENIC homozygous 643896251 2 230398591 230398592 A G 32 GENIC homozygous 643896252