chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 47363495 47363496 T C 22 GENIC homozygous 989239090 15 47363827 47363828 A T 25 GENIC homozygous 989239091 15 47364159 47364160 T C 38 GENIC homozygous 989239092 15 47365187 47365188 A C 32 GENIC homozygous 989239093 15 47366028 47366029 A T 26 GENIC homozygous 989239094 15 47366470 47366471 G T 19 GENIC homozygous 989239095 15 47366514 47366515 C T 16 GENIC homozygous 989239096 15 47366831 47366832 C T 20 GENIC homozygous 989239097 15 47367381 47367382 T C 26 GENIC homozygous 989239098 15 47368113 47368114 T G 5 GENIC homozygous 989239099 15 47368117 47368118 T G 4 GENIC homozygous 989239100 15 47368120 47368121 T G 1 GENIC homozygous 989239101 15 47369067 47369068 G C 36 GENIC homozygous 989239102 15 47369624 47369625 G C 23 GENIC homozygous 989239103 15 47370239 47370240 G T 32 GENIC homozygous 989239104 15 47370518 47370519 G A 35 GENIC homozygous 989239105 15 47370531 47370532 C T 36 GENIC homozygous 989239106 15 47371922 47371923 A G 25 GENIC homozygous 989239107 15 47372395 47372396 A G 31 GENIC homozygous 989239108 15 47372772 47372773 C G 27 GENIC homozygous 989239109 15 47372859 47372860 G A 31 GENIC homozygous 989239110 15 47373812 47373813 G A 35 GENIC homozygous 989239111 15 47374439 47374440 T C 35 GENIC homozygous 989239112 15 47374624 47374625 T C 31 GENIC homozygous 989239113 15 47374861 47374862 A G 31 GENIC homozygous 989239114 15 47375328 47375329 T C 29 GENIC homozygous 989239115 15 47375375 47375376 T C 33 GENIC homozygous 989239116 15 47375604 47375605 T C 36 GENIC homozygous 989239117 15 47375606 47375607 G A 36 GENIC homozygous 989239118 15 47375888 47375889 C T 28 GENIC homozygous 989239119 15 47376209 47376210 G A 36 GENIC homozygous 989239120 15 47376219 47376220 T C 35 GENIC homozygous 989239121 15 47376502 47376503 G A 21 GENIC homozygous 989239122 15 47378500 47378501 A G 36 GENIC homozygous 989239123