chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 13779145 13779146 C T 3 GENIC homozygous 131561258 20 13779155 13779156 T C 4 GENIC homozygous 119770902 20 13779714 13779715 C A 35 GENIC homozygous 119770907 20 13779720 13779721 A T 36 GENIC homozygous 119770909 20 13780470 13780471 C 13 GENIC homozygous 131556732 20 13780790 13780791 A G 35 GENIC homozygous 109100049 20 13781621 13781622 T C 33 GENIC homozygous 109100059 20 13781908 13781909 G 36 GENIC homozygous 131556735 20 13780555 13780555 GCGCGCGCGCGC 13 GENIC homozygous 133591427 20 13781211 13781211 CACA 14 GENIC homozygous 131556733 20 13781905 13781905 TCCAG 35 GENIC homozygous 131556734 20 13781797 13781798 A C 18 GENIC homozygous 109552518 20 13781934 13781935 T C 34 GENIC homozygous 109302613 20 13782128 13782129 C G 46 GENIC homozygous 109100061 20 13782705 13782705 TT 36 GENIC homozygous 129661255 20 13783060 13783061 C T 46 GENIC homozygous 109100065 20 13783792 13783792 G 31 GENIC homozygous 131556736 20 13784262 13784262 G 8 GENIC homozygous 129661257 20 13784266 13784266 GG 9 GENIC homozygous 129661258 20 13784269 13784269 G 9 GENIC homozygous 129661259 20 13784272 13784273 A 9 GENIC homozygous 129661260 20 13784275 13784277 AT 9 GENIC homozygous 129661261 20 13784280 13784284 AAGG 9 GENIC homozygous 129661262 20 13784290 13784290 TG 9 GENIC homozygous 129661263 20 13784300 13784302 GC 9 GENIC homozygous 129661264 20 13782178 13782179 G A 40 GENIC homozygous 109549043 20 13783483 13783484 G C 50 GENIC homozygous 109100067 20 13784464 13784465 A G 21 GENIC homozygous 109100073 20 13782207 13782208 G A 45 GENIC homozygous 109549044 20 13782256 13782257 G C 38 GENIC possibly homozygous 109394282 20 13784293 13784294 T A 9 GENIC homozygous 109456417