chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 109215156 109215160 ACAC ---- 3 GENIC homozygous 694083459 6 109216387 109216389 GT -- 20 GENIC homozygous 694083461 6 109216449 109216450 A C 17 GENIC homozygous 532490070 6 109216711 109216712 C G 13 GENIC homozygous 532490071 6 109217708 109217709 G A 13 GENIC homozygous 532490072 6 109217869 109217870 C CT 7 GENIC heterozygous 694083462 6 109217869 109217870 C CTT 7 GENIC heterozygous 694083463 6 109218078 109218079 T G 16 GENIC homozygous 532490073 6 109218132 109218133 G A 13 GENIC homozygous 532490074 6 109218533 109218534 T C 7 GENIC homozygous 529627474 6 109218971 109218972 C G 9 GENIC homozygous 532490075 6 109219610 109219611 T - 2 GENIC homozygous 694083464 6 109219644 109219645 C G 3 GENIC homozygous 532490076 6 109219945 109219946 G A 21 GENIC homozygous 532490077 6 109220171 109220172 A G 13 GENIC homozygous 529627475 6 109221479 109221480 A G 17 GENIC homozygous 529627476 6 109224251 109224252 C T 23 GENIC homozygous 532490078 6 109224345 109224346 C CTTT 9 GENIC heterozygous 694083465 6 109224345 109224346 C CTT 9 GENIC possibly homozygous 694083466 6 109224503 109224504 C T 29 GENIC possibly homozygous 529627477 6 109225632 109225633 T C 24 GENIC homozygous 529627478 6 109225969 109225970 G C 18 GENIC homozygous 529627479 6 109226303 109226304 G - 11 GENIC homozygous 694083467 6 109226869 109226870 T - 16 GENIC homozygous 694083469 6 109227067 109227069 GA -- 3 GENIC homozygous 694083470 6 109227093 109227094 C CAG 1 GENIC homozygous 694083471 6 109227125 109227126 T G 6 GENIC heterozygous 532490079 6 109227134 109227135 G A 5 GENIC heterozygous 532490080 6 109227301 109227302 C - 18 GENIC heterozygous 694083472 6 109227301 109227302 C CTGTT 13 GENIC homozygous 694083473 6 109227384 109227385 T C 18 GENIC homozygous 529627480 6 109227512 109227513 T A 13 GENIC homozygous 532490081 6 109228010 109228011 G A 20 GENIC homozygous 532490082