chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 56010732 56010733 T C 34 GENIC homozygous 801110233 19 56011013 56011014 C T 47 GENIC homozygous 801110234 19 56011203 56011204 C T 34 GENIC homozygous 801110235 19 56011543 56011544 T C 34 GENIC homozygous 801110236 19 56011979 56011980 C T 34 GENIC homozygous 801110237 19 56012029 56012030 G A 34 GENIC homozygous 801110238 19 56012468 56012469 C A 26 GENIC homozygous 801110239 19 56012835 56012836 T C 39 GENIC homozygous 801110240 19 56014649 56014650 C G 29 GENIC homozygous 801110241 19 56014664 56014665 A G 25 GENIC homozygous 801110242 19 56014888 56014889 A T 33 GENIC homozygous 801110243 19 56015842 56015843 G A 17 GENIC possibly homozygous 801110244 19 56016113 56016114 C A 36 GENIC homozygous 801110245 19 56016888 56016889 G A 34 GENIC homozygous 801110246 19 56017375 56017376 C T 19 GENIC homozygous 801110247 19 56017436 56017437 T A 20 GENIC homozygous 801110248 19 56017846 56017847 T A 16 GENIC homozygous 801110249 19 56017905 56017906 T C 28 GENIC homozygous 801110250 19 56018570 56018571 G A 45 GENIC homozygous 801110251 19 56019292 56019293 T C 40 GENIC homozygous 801110252 19 56019695 56019696 C T 31 GENIC homozygous 801110253 19 56019753 56019754 A G 27 GENIC homozygous 801110254 19 56019944 56019945 C T 24 GENIC homozygous 801110255 19 56020046 56020047 G T 29 GENIC possibly homozygous 801110256 19 56020331 56020332 G A 42 GENIC homozygous 801110257 19 56020497 56020498 T C 35 GENIC homozygous 801110258 19 56021246 56021247 T C 19 GENIC heterozygous 801110259 19 56021265 56021266 T C 17 GENIC homozygous 801110260