chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 144103342 144103343 C G 16 GENIC homozygous 952779551 7 144103528 144103529 T C 15 GENIC homozygous 952779552 7 144103747 144103748 C T 10 GENIC homozygous 952779553 7 144105165 144105166 T G 15 GENIC homozygous 952779554 7 144107661 144107662 A G 25 GENIC homozygous 952779555 7 144107952 144107953 C T 19 GENIC homozygous 952779556 7 144109385 144109386 T C 31 GENIC homozygous 952779557 7 144109598 144109599 C G 37 GENIC homozygous 952779558 7 144109629 144109630 C T 30 GENIC homozygous 952779559 7 144109681 144109682 A C 29 GENIC possibly homozygous 952779560 7 144110529 144110530 C T 23 GENIC homozygous 952779561 7 144110726 144110727 G A 40 GENIC homozygous 952779562 7 144110901 144110902 A C 21 GENIC homozygous 952779563 7 144111438 144111439 T C 24 GENIC homozygous 952779564 7 144112053 144112054 G A 43 GENIC homozygous 952779565 7 144112570 144112571 T C 39 GENIC homozygous 952779566 7 144113830 144113831 A G 12 GENIC homozygous 952779567 7 144115195 144115196 C T 15 GENIC homozygous 952779568 7 144115606 144115607 A G 14 GENIC homozygous 952779569 7 144115720 144115721 G A 21 GENIC homozygous 952779570 7 144115776 144115777 G A 28 GENIC homozygous 952779571 7 144116204 144116205 G A 33 GENIC homozygous 952779572 7 144116838 144116839 G A 21 GENIC homozygous 952779573 7 144116920 144116921 T C 21 GENIC homozygous 952779574