chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 189829747 189829748 T C 32 GENIC homozygous 797658326 2 189829929 189829930 T C 30 GENIC homozygous 797658327 2 189829990 189829991 C T 22 GENIC homozygous 797658328 2 189830468 189830469 T A 21 GENIC homozygous 797658329 2 189830476 189830477 A C 22 GENIC homozygous 797658330 2 189830617 189830618 C G 33 GENIC possibly homozygous 797658331 2 189830864 189830865 A G 37 GENIC heterozygous 797658332 2 189831061 189831062 C T 32 GENIC homozygous 797658333 2 189831619 189831620 C T 21 GENIC homozygous 797658334 2 189831649 189831650 G A 22 GENIC homozygous 797658335 2 189832252 189832253 G A 44 GENIC homozygous 797658336 2 189832513 189832514 G A 38 GENIC possibly homozygous 797658337 2 189832825 189832826 C G 19 GENIC heterozygous 797658338 2 189832888 189832889 G A 39 GENIC heterozygous 797658339 2 189832938 189832939 T C 66 GENIC heterozygous 797658340 2 189833106 189833107 T A 249 GENIC heterozygous 797658341 2 189833110 189833111 G T 250 GENIC heterozygous 797658342 2 189833762 189833763 G A 11 GENIC homozygous 797658343 2 189833886 189833887 C T 28 GENIC homozygous 797658344 2 189833916 189833917 A C 27 GENIC homozygous 797658345 2 189834736 189834737 A G 31 GENIC possibly homozygous 797658346