chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 56010732 56010733 T C 26 GENIC homozygous 992369276 19 56011013 56011014 C T 29 GENIC homozygous 992369277 19 56011203 56011204 C T 27 GENIC homozygous 992369278 19 56011543 56011544 T C 17 GENIC homozygous 992369279 19 56011979 56011980 C T 19 GENIC homozygous 992369280 19 56012029 56012030 G A 18 GENIC homozygous 992369281 19 56012468 56012469 C A 24 GENIC homozygous 992369282 19 56012835 56012836 T C 23 GENIC homozygous 992369283 19 56014649 56014650 C G 19 GENIC homozygous 992369284 19 56014664 56014665 A G 20 GENIC homozygous 992369285 19 56014888 56014889 A T 16 GENIC homozygous 992369286 19 56016888 56016889 G A 20 GENIC homozygous 992369287 19 56017436 56017437 T A 17 GENIC homozygous 992369288 19 56017846 56017847 T A 19 GENIC homozygous 992369289 19 56017905 56017906 T C 17 GENIC homozygous 992369290 19 56018570 56018571 G A 21 GENIC homozygous 992369291 19 56019292 56019293 T C 14 GENIC homozygous 992369292 19 56019695 56019696 C T 17 GENIC homozygous 992369293 19 56019753 56019754 A G 15 GENIC homozygous 992369294 19 56019944 56019945 C T 8 GENIC homozygous 992369295 19 56020331 56020332 G A 15 GENIC homozygous 992369296 19 56020497 56020498 T C 18 GENIC homozygous 992369297