chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 205128834 205128835 G A 25 GENIC homozygous 515760145 4 205129264 205129265 A G 31 GENIC homozygous 515760146 4 205129586 205129587 T TG 27 GENIC homozygous 688983679 4 205129782 205129783 T C 22 GENIC homozygous 515760147 4 205129956 205129957 C T 31 GENIC homozygous 515760148 4 205130304 205130305 C T 26 GENIC possibly homozygous 515760149 4 205130305 205130306 T C 26 GENIC possibly homozygous 515760150 4 205130578 205130579 C T 22 GENIC homozygous 515760151 4 205130927 205130928 C G 24 GENIC homozygous 515760152 4 205131056 205131057 T C 26 GENIC homozygous 515760153 4 205131067 205131068 A G 24 GENIC homozygous 515760154 4 205131439 205131440 G C 21 GENIC homozygous 515760155 4 205132557 205132558 G A 39 GENIC homozygous 519037754 4 205132645 205132646 G A 24 GENIC homozygous 515760156 4 205133039 205133040 A G 16 GENIC homozygous 515760157 4 205133447 205133448 G A 20 GENIC homozygous 515760158 4 205134011 205134012 T C 17 GENIC homozygous 515760159 4 205137895 205137896 A ATAAG 1 GENIC homozygous 688983680 4 205138221 205138222 T C 17 GENIC homozygous 515760160 4 205138227 205138228 G GTTT 15 GENIC possibly homozygous 688983681 4 205138227 205138228 G GTT 15 GENIC heterozygous 688983682 4 205149823 205149824 T C 26 GENIC homozygous 515760161 4 205149920 205149921 T A 31 GENIC homozygous 515760162