chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 14653911 14653912 G T 35 GENIC homozygous 971331396 19 14654618 14654619 C T 29 GENIC homozygous 971331397 19 14654824 14654825 G A 29 GENIC homozygous 971331398 19 14656129 14656130 C T 29 GENIC homozygous 971331399 19 14657553 14657554 A G 42 GENIC homozygous 971331400 19 14658363 14658364 T C 32 GENIC homozygous 971331401 19 14658871 14658872 A G 29 GENIC homozygous 971331402 19 14659256 14659257 A T 30 GENIC homozygous 971331403 19 14659420 14659421 A G 34 GENIC homozygous 971331404 19 14659786 14659787 A T 39 GENIC homozygous 971331405 19 14660773 14660774 A G 35 GENIC homozygous 971331406 19 14662466 14662467 A C 29 GENIC homozygous 971331407 19 14662467 14662468 G A 29 GENIC homozygous 971331408 19 14662927 14662928 T C 32 GENIC homozygous 971331409 19 14663545 14663546 A G 33 GENIC homozygous 971331410 19 14663776 14663777 T C 35 GENIC homozygous 971331411