chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 220111578 220111579 A G 36 GENIC homozygous 640917904 4 220111690 220111691 G A 19 GENIC homozygous 640917905 4 220112075 220112076 C T 23 GENIC homozygous 640917906 4 220112207 220112208 G A 21 GENIC homozygous 640917907 4 220112789 220112790 G GT 20 GENIC homozygous 751579589 4 220113056 220113057 A AGGG 23 GENIC homozygous 751579590 4 220113334 220113335 C T 16 GENIC homozygous 640917908 4 220113358 220113359 A AT 12 GENIC heterozygous 751579591 4 220113358 220113359 A ATT 12 GENIC heterozygous 751579592 4 220113358 220113359 A ATTTTTTT 12 GENIC heterozygous 751579593 4 220113396 220113397 T C 14 GENIC homozygous 640917909 4 220113407 220113408 C T 16 GENIC homozygous 640917910 4 220113576 220113577 A T 19 GENIC homozygous 640917911 4 220113690 220113691 A ACACACGCACACG 12 GENIC homozygous 751579594 4 220113907 220113908 C T 23 GENIC homozygous 640917912 4 220114108 220114109 T TGGTGGTGGAGGA 14 GENIC homozygous 751579598 4 220114252 220114253 C T 25 GENIC homozygous 640917913 4 220114486 220114487 C G 18 GENIC homozygous 640917914 4 220115702 220115703 G C 15 GENIC homozygous 640917915 4 220116303 220116304 T TCTACACAATACCTTTTTTTTTTTTTTTTTTGGTTCTGTTTTTCG 10 GENIC homozygous 751579599 4 220116735 220116736 C T 20 GENIC homozygous 640917916