chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 155593660 155593661 G - 17 GENIC homozygous 56993552 4 155593743 155593744 G - 16 GENIC homozygous 56993553 4 155593749 155593750 G - 17 GENIC homozygous 56993554 4 155594736 155594737 C CTTGG 20 GENIC homozygous 56993565 4 155597318 155597319 T TTCATG 22 GENIC homozygous 56993583 4 155598102 155598103 C T 25 GENIC heterozygous 56993585 4 155599646 155599647 C G 16 GENIC heterozygous 56993597 4 155603387 155603388 A T 29 GENIC homozygous 56993635 4 155619170 155619171 G A 37 GENIC homozygous 56993695 4 155624988 155624989 T C 24 GENIC homozygous 56993719 4 155636179 155636181 AC -- 7 GENIC heterozygous 58348297 4 155646605 155646606 G GCTGCT 23 GENIC homozygous 58287261 4 155648380 155648381 A - 12 GENIC homozygous 56993721 4 155656069 155656072 GGG --- 1 GENIC homozygous 56993730 4 155662991 155662992 G GGT 17 GENIC heterozygous 57526512 4 155682858 155682859 G A 28 GENIC heterozygous 59133936 4 155682866 155682867 T A 27 GENIC heterozygous 59133938 4 155683029 155683030 T C 15 GENIC heterozygous 59133944 4 155683034 155683035 C G 15 GENIC heterozygous 59133946 4 155684072 155684073 T - 7 GENIC heterozygous 59133970