chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 205128834 205128835 G A 17 GENIC homozygous 621541180 4 205129264 205129265 A G 22 GENIC homozygous 621541181 4 205129586 205129587 T TG 19 GENIC homozygous 739335251 4 205129782 205129783 T C 15 GENIC homozygous 621541182 4 205129956 205129957 C T 19 GENIC homozygous 621541183 4 205130242 205130243 C T 20 GENIC homozygous 621541184 4 205130304 205130305 C T 24 GENIC homozygous 621541185 4 205130305 205130306 T C 24 GENIC homozygous 621541186 4 205130578 205130579 C T 17 GENIC homozygous 621541187 4 205130927 205130928 C G 16 GENIC homozygous 621541188 4 205131056 205131057 T C 24 GENIC homozygous 621541189 4 205131067 205131068 A G 27 GENIC homozygous 621541190 4 205131439 205131440 G C 28 GENIC homozygous 621541191 4 205132645 205132646 G A 13 GENIC homozygous 621541192 4 205133026 205133027 G A 18 GENIC homozygous 621541193 4 205133039 205133040 A G 18 GENIC homozygous 621541194 4 205133447 205133448 G A 21 GENIC homozygous 621541195 4 205133966 205133967 C T 12 GENIC homozygous 621541196 4 205134011 205134012 T C 12 GENIC homozygous 621541197 4 205134854 205134855 C T 24 GENIC homozygous 621541198 4 205135577 205135578 C T 21 GENIC homozygous 621541199 4 205137912 205137913 C T 1 GENIC homozygous 621541200 4 205138221 205138222 T C 16 GENIC homozygous 621541201 4 205138227 205138228 G GTT 19 GENIC possibly homozygous 739335252 4 205138227 205138228 G GTTT 19 GENIC heterozygous 739335253 4 205149823 205149824 T C 28 GENIC homozygous 621541202 4 205149920 205149921 T A 35 GENIC homozygous 621541203