chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 137253641 137253642 G A 68 GENIC homozygous 137632602 5 137253876 137253877 T A 53 GENIC possibly homozygous 137632603 5 137254142 137254143 T G 60 GENIC homozygous 137632604 5 137255545 137255546 T C 75 GENIC homozygous 137632605 5 137259401 137259401 C 11 GENIC homozygous 137344493 5 137259956 137259957 C T 48 GENIC homozygous 137632606 5 137261171 137261172 G T 60 GENIC homozygous 137632607 5 137265190 137265191 G A 35 GENIC homozygous 137632608 5 137268262 137268263 C T 61 GENIC homozygous 137632609 5 137268361 137268362 C T 59 GENIC homozygous 137632610 5 137268802 137268803 T G 52 GENIC homozygous 137632611 5 137269102 137269103 T C 68 GENIC homozygous 137632612 5 137269274 137269275 C T 61 GENIC homozygous 137632613 5 137271910 137271911 G A 55 GENIC homozygous 137632614 5 137272049 137272050 G A 49 GENIC homozygous 137632615 5 137272231 137272232 A G 57 GENIC homozygous 137632616 5 137272535 137272537 CA 32 GENIC homozygous 137344494 5 137272699 137272700 C T 42 GENIC homozygous 137632617 5 137272719 137272720 C A 44 GENIC homozygous 137632618 5 137273040 137273041 T A 38 GENIC possibly homozygous 137632619 5 137273079 137273080 A G 36 GENIC homozygous 137632620 5 137273246 137273247 A T 49 GENIC homozygous 137632621 5 137273247 137273248 A T 49 GENIC homozygous 137632622