chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 144103342 144103343 C G 20 GENIC homozygous 967221379 7 144103528 144103529 T C 27 GENIC possibly homozygous 967221380 7 144105165 144105166 T G 25 GENIC homozygous 967221381 7 144107661 144107662 A G 34 GENIC homozygous 967221382 7 144107952 144107953 C T 34 GENIC homozygous 967221383 7 144109385 144109386 T C 49 GENIC possibly homozygous 967221384 7 144109598 144109599 C G 41 GENIC homozygous 967221385 7 144109629 144109630 C T 38 GENIC homozygous 967221386 7 144109681 144109682 A C 35 GENIC homozygous 967221387 7 144110529 144110530 C T 34 GENIC possibly homozygous 967221388 7 144110726 144110727 G A 42 GENIC homozygous 967221389 7 144110901 144110902 A C 48 GENIC homozygous 967221390 7 144111438 144111439 T C 29 GENIC homozygous 967221391 7 144112053 144112054 G A 31 GENIC homozygous 967221392 7 144112570 144112571 T C 49 GENIC homozygous 967221393 7 144115195 144115196 C T 31 GENIC homozygous 967221394 7 144115720 144115721 G A 37 GENIC homozygous 967221395 7 144115776 144115777 G A 43 GENIC homozygous 967221396 7 144116204 144116205 G A 49 GENIC homozygous 967221397 7 144116838 144116839 G A 31 GENIC homozygous 967221398 7 144116920 144116921 T C 28 GENIC homozygous 967221399