chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 14654618 14654619 C T 18 GENIC homozygous 891203699 19 14654824 14654825 G A 9 GENIC homozygous 891203700 19 14654826 14654827 G A 9 GENIC homozygous 891203701 19 14655942 14655943 C T 19 GENIC homozygous 891203702 19 14656676 14656677 G A 10 GENIC homozygous 891203703 19 14657553 14657554 A G 9 GENIC homozygous 891203704 19 14657578 14657579 C T 10 GENIC homozygous 891203705 19 14658363 14658364 T C 9 GENIC homozygous 891203706 19 14659257 14659258 C T 11 GENIC homozygous 891203707 19 14659347 14659348 G A 9 GENIC homozygous 891203708 19 14659420 14659421 A G 12 GENIC homozygous 891203709 19 14659588 14659589 C T 13 GENIC homozygous 891203710 19 14660318 14660319 G A 5 GENIC homozygous 891203711 19 14661428 14661429 T A 12 GENIC homozygous 891203712 19 14662496 14662497 A G 10 GENIC homozygous 891203713 19 14662927 14662928 T C 12 GENIC homozygous 891203714 19 14663545 14663546 A G 5 GENIC homozygous 891203715 19 14663776 14663777 T C 11 GENIC homozygous 891203716