chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 56010732 56010733 T C 22 GENIC homozygous 942636448 19 56011013 56011014 C T 19 GENIC homozygous 942636449 19 56011203 56011204 C T 35 GENIC homozygous 942636450 19 56011543 56011544 T C 35 GENIC homozygous 942636451 19 56011979 56011980 C T 16 GENIC homozygous 942636452 19 56012029 56012030 G A 12 GENIC homozygous 942636453 19 56012468 56012469 C A 38 GENIC homozygous 942636454 19 56012835 56012836 T C 22 GENIC homozygous 942636455 19 56014649 56014650 C G 13 GENIC homozygous 942636456 19 56014664 56014665 A G 11 GENIC homozygous 942636457 19 56014888 56014889 A T 31 GENIC homozygous 942636458 19 56016113 56016114 C A 24 GENIC homozygous 942636459 19 56016888 56016889 G A 22 GENIC homozygous 942636460 19 56017436 56017437 T A 15 GENIC homozygous 942636461 19 56017846 56017847 T A 18 GENIC homozygous 942636462 19 56017905 56017906 T C 18 GENIC homozygous 942636463 19 56018570 56018571 G A 32 GENIC homozygous 942636464 19 56019292 56019293 T C 22 GENIC homozygous 942636465 19 56019695 56019696 C T 23 GENIC homozygous 942636466 19 56019753 56019754 A G 23 GENIC homozygous 942636467 19 56019944 56019945 C T 20 GENIC homozygous 942636468 19 56020331 56020332 G A 23 GENIC homozygous 942636469 19 56020497 56020498 T C 32 GENIC homozygous 942636470 19 56021385 56021386 C A 17 GENIC homozygous 942636471