chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 144103342 144103343 C G 33 GENIC homozygous 970082015 7 144103528 144103529 T C 23 GENIC homozygous 970082016 7 144105165 144105166 T G 31 GENIC homozygous 970082017 7 144107661 144107662 A G 30 GENIC homozygous 970082018 7 144107952 144107953 C T 31 GENIC homozygous 970082019 7 144109385 144109386 T C 34 GENIC homozygous 970082020 7 144109598 144109599 C G 35 GENIC homozygous 970082021 7 144109629 144109630 C T 37 GENIC homozygous 970082022 7 144109681 144109682 A C 44 GENIC homozygous 970082023 7 144110529 144110530 C T 34 GENIC homozygous 970082024 7 144110901 144110902 A C 42 GENIC homozygous 970082025 7 144111438 144111439 T C 42 GENIC homozygous 970082026 7 144112053 144112054 G A 19 GENIC homozygous 970082027 7 144112570 144112571 T C 27 GENIC homozygous 970082028 7 144113830 144113831 A G 47 GENIC homozygous 970082029 7 144115195 144115196 C T 30 GENIC homozygous 970082030 7 144115606 144115607 A G 29 GENIC homozygous 970082031 7 144115720 144115721 G A 21 GENIC homozygous 970082032 7 144115776 144115777 G A 17 GENIC homozygous 970082033 7 144116204 144116205 G A 47 GENIC homozygous 970082034 7 144116838 144116839 G A 22 GENIC homozygous 970082035 7 144116920 144116921 T C 19 GENIC homozygous 970082036