chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 20795053 20795054 A G 17 GENIC homozygous 110985959 17 20797667 20797668 T C 13 GENIC homozygous 111177707 17 20797774 20797775 T A 13 GENIC homozygous 111177709 17 20797889 20797890 T C 19 GENIC homozygous 110985961 17 20797949 20797950 T C 26 GENIC homozygous 110985963 17 20797950 20797951 T C 26 GENIC homozygous 110985965 17 20798841 20798842 C G 19 GENIC homozygous 110985967 17 20798894 20798895 T C 16 GENIC homozygous 110985969 17 20798907 20798908 C T 20 GENIC homozygous 110985971 17 20799056 20799057 A G 15 GENIC homozygous 110985973 17 20807454 20807455 A C 16 GENIC homozygous 110985975 17 20807576 20807577 G A 14 GENIC homozygous 110985977 17 20807669 20807670 T G 9 GENIC homozygous 110985979 17 20807749 20807750 A T 16 GENIC homozygous 110985981 17 20808718 20808719 G A 17 GENIC homozygous 110985983 17 20809044 20809045 G A 20 GENIC homozygous 110985985 17 20809177 20809178 C T 17 GENIC homozygous 110985987 17 20809223 20809224 T C 15 GENIC homozygous 110985989 17 20810150 20810151 T C 23 GENIC homozygous 110985991 17 20811997 20811998 T C 35 GENIC homozygous 110985993 17 20812293 20812294 T C 23 GENIC homozygous 110985995 17 20812941 20812942 C T 18 GENIC homozygous 110985997 17 20813294 20813295 G A 7 GENIC homozygous 110985999