chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 205128834 205128835 G A 33 GENIC homozygous 572531490 4 205129264 205129265 A G 34 GENIC homozygous 572531491 4 205129586 205129587 T TG 41 GENIC homozygous 714166272 4 205129782 205129783 T C 17 GENIC homozygous 572531492 4 205129956 205129957 C T 22 GENIC homozygous 572531493 4 205130242 205130243 C T 17 GENIC homozygous 572531494 4 205130304 205130305 C T 28 GENIC homozygous 572531495 4 205130305 205130306 T C 28 GENIC homozygous 572531496 4 205130578 205130579 C T 19 GENIC homozygous 572531497 4 205130927 205130928 C G 18 GENIC homozygous 572531498 4 205131056 205131057 T C 17 GENIC homozygous 572531499 4 205131067 205131068 A G 16 GENIC homozygous 572531500 4 205131439 205131440 G C 29 GENIC homozygous 572531501 4 205132645 205132646 G A 29 GENIC homozygous 572531502 4 205133026 205133027 G A 25 GENIC homozygous 575134057 4 205133039 205133040 A G 22 GENIC homozygous 572531503 4 205133447 205133448 G A 20 GENIC homozygous 572531504 4 205133966 205133967 C T 12 GENIC homozygous 572531505 4 205134011 205134012 T C 13 GENIC homozygous 572531506 4 205134854 205134855 C T 20 GENIC homozygous 572531507 4 205135577 205135578 C T 18 GENIC homozygous 572531508 4 205138221 205138222 T C 10 GENIC homozygous 572531509 4 205138227 205138228 G GTT 9 GENIC possibly homozygous 714166273 4 205138227 205138228 G GTTT 9 GENIC heterozygous 714166274 4 205149823 205149824 T C 26 GENIC homozygous 572531510 4 205149920 205149921 T A 24 GENIC homozygous 572531511