chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 100417353 100417354 G A 15 GENIC homozygous 113689052 14 100417489 100417490 G A 17 GENIC homozygous 113689054 14 100417537 100417538 G T 18 GENIC homozygous 113520967 14 100417733 100417734 T A 21 GENIC homozygous 113520971 14 100417792 100417793 A C 12 GENIC homozygous 113520973 14 100417793 100417794 C A 13 GENIC homozygous 113520975 14 100417885 100417886 T C 11 GENIC homozygous 113520977 14 100417886 100417887 C T 10 GENIC homozygous 113520979 14 100418436 100418437 C A 14 GENIC homozygous 113520981 14 100419125 100419126 C T 24 GENIC homozygous 113520983 14 100419126 100419127 A G 24 GENIC homozygous 113520985 14 100420053 100420054 T G 41 GENIC homozygous 113520987 14 100420380 100420381 A G 10 GENIC homozygous 113520989 14 100420423 100420424 C G 17 GENIC homozygous 113520991 14 100420998 100420999 A G 17 GENIC homozygous 113520993 14 100421006 100421007 A G 16 GENIC homozygous 113520995 14 100421122 100421123 A G 33 GENIC homozygous 113520997 14 100421446 100421447 T G 22 GENIC homozygous 113520999 14 100421730 100421731 A T 7 GENIC homozygous 113689058 14 100423233 100423234 T C 9 GENIC homozygous 113689060 14 100423870 100423871 C T 23 GENIC homozygous 113689062 14 100424249 100424250 C T 10 GENIC homozygous 113521003 14 100424489 100424490 T C 3 GENIC homozygous 113521005 14 100422999 100423000 G A 18 GENIC homozygous 113764179 14 100423522 100423523 G A 13 GENIC homozygous 113764181 14 100424126 100424127 G A 26 GENIC homozygous 113764183