chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 9418477 9418478 G A 14 GENIC homozygous 63356266 20 9418778 9418779 G T 5 GENIC homozygous 63786071 20 9418794 9418795 T G 3 GENIC homozygous 63786073 20 9419309 9419310 C G 26 GENIC homozygous 63356268 20 9419473 9419474 G A 35 GENIC homozygous 63582182 20 9419538 9419539 C T 35 GENIC possibly homozygous 63356270 20 9419719 9419720 T C 22 GENIC homozygous 63356272 20 9420706 9420707 A G 21 GENIC homozygous 63356274 20 9420984 9420985 C T 26 GENIC homozygous 63356276 20 9421452 9421453 G A 20 GENIC homozygous 63356278 20 9422294 9422295 C T 38 GENIC homozygous 63356280 20 9422415 9422416 G A 14 GENIC homozygous 63356282 20 9422475 9422476 G T 17 GENIC homozygous 63356284 20 9422138 9422139 T C 3 GENIC homozygous 63741271