chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 55706280 55706281 A T 38 GENIC homozygous 974289642 19 55707333 55707334 T C 28 GENIC homozygous 974289643 19 55708126 55708127 T C 35 GENIC homozygous 974289644 19 55710362 55710363 G A 22 GENIC homozygous 974289645 19 55710776 55710777 G A 37 GENIC homozygous 974289646 19 55714226 55714227 T C 38 GENIC homozygous 974289647 19 55714448 55714449 C T 24 GENIC possibly homozygous 974289648 19 55717078 55717079 A G 23 GENIC homozygous 974289649 19 55719614 55719615 T C 26 GENIC homozygous 974289650 19 55720010 55720011 C A 20 GENIC homozygous 974289651 19 55722613 55722614 G C 24 GENIC homozygous 974289652 19 55738389 55738390 T C 35 GENIC homozygous 974289653 19 55749482 55749483 C A 22 GENIC homozygous 974289654 19 55780593 55780594 C T 28 GENIC homozygous 974289655 19 55781108 55781109 A C 31 GENIC homozygous 974289656 19 55858539 55858540 G T 13 GENIC homozygous 974289657