chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 56010732 56010733 T C 25 GENIC homozygous 953741269 19 56011013 56011014 C T 22 GENIC homozygous 953741270 19 56011203 56011204 C T 21 GENIC homozygous 953741271 19 56011543 56011544 T C 27 GENIC homozygous 953741272 19 56011979 56011980 C T 23 GENIC homozygous 953741273 19 56012029 56012030 G A 29 GENIC homozygous 953741274 19 56012468 56012469 C A 33 GENIC homozygous 953741275 19 56012835 56012836 T C 29 GENIC homozygous 953741276 19 56014649 56014650 C G 26 GENIC homozygous 953741277 19 56014664 56014665 A G 23 GENIC homozygous 953741278 19 56014888 56014889 A T 22 GENIC homozygous 953741279 19 56016113 56016114 C A 20 GENIC homozygous 953741280 19 56016888 56016889 G A 29 GENIC homozygous 953741281 19 56017436 56017437 T A 25 GENIC homozygous 953741282 19 56017846 56017847 T A 23 GENIC homozygous 953741283 19 56017905 56017906 T C 15 GENIC homozygous 953741284 19 56018570 56018571 G A 17 GENIC homozygous 953741285 19 56019292 56019293 T C 15 GENIC homozygous 953741286 19 56019695 56019696 C T 41 GENIC homozygous 953741287 19 56019753 56019754 A G 32 GENIC homozygous 953741288 19 56019944 56019945 C T 23 GENIC homozygous 953741289 19 56020331 56020332 G A 29 GENIC homozygous 953741290 19 56020497 56020498 T C 22 GENIC homozygous 953741291