chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 47363495 47363496 T C 18 GENIC homozygous 986352091 15 47364024 47364025 T C 21 GENIC homozygous 986352092 15 47364159 47364160 T C 31 GENIC homozygous 986352093 15 47365187 47365188 A C 16 GENIC homozygous 986352094 15 47366028 47366029 A T 25 GENIC homozygous 986352095 15 47366470 47366471 G T 13 GENIC homozygous 986352096 15 47366514 47366515 C T 14 GENIC homozygous 986352097 15 47367381 47367382 T C 22 GENIC homozygous 986352098 15 47367627 47367628 A C 21 GENIC homozygous 986352099 15 47369067 47369068 G C 22 GENIC homozygous 986352100 15 47369624 47369625 G C 22 GENIC homozygous 986352101 15 47370239 47370240 G T 18 GENIC homozygous 986352102 15 47370518 47370519 G A 22 GENIC homozygous 986352103 15 47370531 47370532 C T 26 GENIC homozygous 986352104 15 47371922 47371923 A G 17 GENIC homozygous 986352105 15 47372395 47372396 A G 17 GENIC homozygous 986352106 15 47372772 47372773 C G 14 GENIC homozygous 986352107 15 47372859 47372860 G A 24 GENIC homozygous 986352108 15 47373812 47373813 G A 12 GENIC homozygous 986352109 15 47374439 47374440 T C 21 GENIC homozygous 986352110 15 47374624 47374625 T C 13 GENIC homozygous 986352111 15 47374861 47374862 A G 28 GENIC homozygous 986352112 15 47375328 47375329 T C 23 GENIC homozygous 986352113 15 47375375 47375376 T C 29 GENIC homozygous 986352114 15 47375604 47375605 T C 20 GENIC homozygous 986352115 15 47375606 47375607 G A 19 GENIC homozygous 986352116 15 47375888 47375889 C T 26 GENIC homozygous 986352117 15 47376209 47376210 G A 21 GENIC homozygous 986352118 15 47376219 47376220 T C 23 GENIC homozygous 986352119 15 47376502 47376503 G A 14 GENIC homozygous 986352120 15 47378500 47378501 A G 17 GENIC homozygous 986352121