chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 220111578 220111579 A G 19 GENIC possibly homozygous 562570757 4 220111690 220111691 G A 22 GENIC homozygous 562570758 4 220112075 220112076 C T 24 GENIC possibly homozygous 562570759 4 220112207 220112208 G A 14 GENIC possibly homozygous 562570760 4 220112789 220112790 G GT 12 GENIC homozygous 708254457 4 220113056 220113057 A AGGG 2 GENIC homozygous 708254458 4 220113334 220113335 C T 13 GENIC homozygous 562570761 4 220113358 220113359 A ATT 1 GENIC homozygous 708254460 4 220113396 220113397 T C 10 GENIC homozygous 562570762 4 220113407 220113408 C T 11 GENIC homozygous 562570763 4 220113576 220113577 A T 25 GENIC homozygous 562570764 4 220113907 220113908 C T 12 GENIC homozygous 565013856 4 220114108 220114109 T TGGTGGTGGAGGA 1 GENIC homozygous 708254462 4 220114252 220114253 C T 13 GENIC homozygous 565013857 4 220114486 220114487 C G 14 GENIC possibly homozygous 562570765 4 220116303 220116304 T TCTACACAATACCTTTTTTTTTTTTTTTTTTGGTTCTGTTTTTCG 2 GENIC heterozygous 708254463 4 220116735 220116736 C T 24 GENIC possibly homozygous 565013858