chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 18399161 18399162 T C 57 GENIC homozygous 112464139 15 18399488 18399489 G A 50 GENIC homozygous 112464141 15 18400146 18400147 G A 44 GENIC homozygous 112464143 15 18407029 18407030 T 41 GENIC homozygous 129234597 15 18406958 18406958 A 33 GENIC homozygous 129234591 15 18406973 18406974 T 35 GENIC homozygous 129234592 15 18406975 18406976 T 35 GENIC homozygous 129234593 15 18406986 18406989 GGT 37 GENIC homozygous 129234594 15 18407003 18407004 A 35 GENIC homozygous 129234595 15 18407026 18407028 AT 41 GENIC homozygous 129234596 15 18406981 18406982 A G 36 GENIC homozygous 112999733 15 18407039 18407040 G 42 GENIC homozygous 129234598 15 18407046 18407047 A 44 GENIC homozygous 129234599 15 18407049 18407050 G C 44 GENIC homozygous 112999737 15 18411043 18411043 TT 12 GENIC homozygous 129234600 15 18411059 18411059 C 13 GENIC homozygous 129234601 15 18411078 18411079 C 22 GENIC homozygous 129234602 15 18411080 18411081 C 23 GENIC homozygous 129234603 15 18411122 18411123 C 34 GENIC homozygous 129234604 15 18411131 18411137 GGGCCG 35 GENIC homozygous 129234605 15 18411378 18411379 C 38 GENIC homozygous 129234606 15 18411388 18411389 G A 38 GENIC homozygous 112464145 15 18411393 18411394 G 40 GENIC homozygous 129234607 15 18411395 18411396 G T 40 GENIC homozygous 112464147 15 18411400 18411401 C A 39 GENIC homozygous 112464149 15 18411412 18411413 G T 37 GENIC homozygous 112464151 15 18411431 18411432 A T 37 GENIC homozygous 112464153 15 18411437 18411437 C 37 GENIC homozygous 129234608 15 18411442 18411443 A 38 GENIC homozygous 129234609 15 18415925 18415928 AAT 43 GENIC homozygous 129234610 15 18415941 18415942 C 44 GENIC homozygous 129234611 15 18415947 18415947 T 46 GENIC homozygous 129234612