chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 105019640 105019641 A G 11 GENIC homozygous 891862472 2 105019997 105019998 T G 18 GENIC homozygous 891862473 2 105020239 105020240 C T 16 GENIC homozygous 891862474 2 105020353 105020354 G A 29 GENIC homozygous 891862475 2 105027043 105027044 A G 9 GENIC homozygous 891864037 2 105027154 105027155 T C 14 GENIC homozygous 891864038 2 105027389 105027390 C G 31 GENIC homozygous 891864039 2 105029111 105029112 G A 19 GENIC homozygous 891862476 2 105029318 105029319 C A 21 GENIC homozygous 891862477 2 105029571 105029572 G C 14 GENIC homozygous 891862478 2 105029712 105029713 T C 5 GENIC homozygous 891862479 2 105029715 105029716 A G 6 GENIC homozygous 891862480 2 105029862 105029863 T C 14 GENIC homozygous 891862481 2 105030086 105030087 T A 7 GENIC homozygous 891862482 2 105030109 105030110 G C 5 GENIC homozygous 891862483 2 105030787 105030788 T C 9 GENIC homozygous 891862484 2 105035830 105035831 C T 22 GENIC homozygous 891862485 2 105040151 105040152 G A 7 GENIC homozygous 891862486 2 105041199 105041200 T C 18 GENIC homozygous 891862487 2 105042291 105042292 T C 15 GENIC homozygous 891862488 2 105044361 105044362 A G 11 GENIC homozygous 891862489 2 105044760 105044761 A T 8 GENIC homozygous 891862490 2 105045764 105045765 T G 12 GENIC homozygous 891862491 2 105046224 105046225 C A 16 GENIC homozygous 891862492 2 105047252 105047253 G A 12 GENIC homozygous 891862493