chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 6655474 6655475 T A 13 GENIC homozygous 47717940 16 6656025 6656026 C T 17 GENIC homozygous 47717941 16 6656880 6656881 A G 18 GENIC homozygous 47256073 16 6656941 6656942 A G 21 GENIC possibly homozygous 47717942 16 6657076 6657077 G A 35 GENIC possibly homozygous 47717943 16 6657130 6657131 G C 26 GENIC homozygous 47256074 16 6657191 6657192 A G 19 GENIC homozygous 47256075 16 6657356 6657357 T C 22 GENIC homozygous 47717945 16 6657848 6657849 T C 16 GENIC possibly homozygous 47717946 16 6658934 6658935 T A 19 GENIC possibly homozygous 47256080 16 6659223 6659224 T C 25 GENIC homozygous 47256081 16 6659506 6659507 T C 12 GENIC homozygous 47256082 16 6659710 6659711 C CCT 6 GENIC homozygous 47256084 16 6661344 6661345 T C 13 GENIC possibly homozygous 47256088 16 6661388 6661389 T C 6 GENIC homozygous 47797371 16 6661633 6661634 T C 13 GENIC possibly homozygous 47256089 16 6663409 6663410 T C 19 GENIC homozygous 47256092 16 6663438 6663439 T C 18 GENIC possibly homozygous 47717947 16 6664233 6664234 A G 8 GENIC heterozygous 47256093 16 6665178 6665182 CACG ---- 5 GENIC heterozygous 47256097 16 6666028 6666029 A G 7 GENIC heterozygous 47717950 16 6670538 6670539 T C 10 GENIC homozygous 47256107 16 6672381 6672382 A C 19 GENIC heterozygous 47256109 16 6673155 6673156 G A 22 GENIC homozygous 47717952 16 6673356 6673357 A - 1 GENIC homozygous 47797397 16 6675577 6675578 A G 3 GENIC homozygous 47717954 16 6661386 6661387 C T 5 GENIC homozygous 47605382 16 6665169 6665170 C G 6 GENIC homozygous 47901113