chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 142110094 142110095 T A 59 GENIC homozygous 115941385 7 142110596 142110596 TGT 65 GENIC homozygous 128530284 7 142115031 142115032 C T 59 GENIC homozygous 115941386 7 142116047 142116048 C T 68 GENIC homozygous 115941387 7 142116249 142116250 T C 61 GENIC homozygous 115941388 7 142116258 142116259 C T 62 GENIC homozygous 115941389 7 142116263 142116264 T C 62 GENIC homozygous 115941390 7 142116946 142116947 A G 46 GENIC homozygous 115941391 7 142117451 142117451 C 42 GENIC homozygous 128530285 7 142117867 142117879 GTGCGTGTGCGC 55 GENIC homozygous 128530286 7 142117987 142117987 GC 54 GENIC homozygous 128530287 7 142118006 142118007 C T 56 GENIC homozygous 115941393 7 142119389 142119390 A G 70 GENIC homozygous 115941394 7 142119473 142119474 C T 55 GENIC possibly homozygous 115941395 7 142119769 142119770 C G 60 GENIC homozygous 115941396 7 142117920 142117921 T C 53 GENIC homozygous 128564223 7 142117978 142117979 C T 56 GENIC homozygous 128564224