chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 14654618 14654619 C T 26 GENIC homozygous 894634498 19 14654824 14654825 G A 9 GENIC homozygous 894634499 19 14654826 14654827 G A 9 GENIC homozygous 894634500 19 14655942 14655943 C T 31 GENIC homozygous 894634501 19 14656129 14656130 C T 9 GENIC homozygous 894634502 19 14656676 14656677 G A 11 GENIC homozygous 894634503 19 14657553 14657554 A G 11 GENIC homozygous 894634504 19 14657578 14657579 C T 14 GENIC homozygous 894634505 19 14658363 14658364 T C 19 GENIC homozygous 894634506 19 14659257 14659258 C T 12 GENIC homozygous 894634507 19 14659347 14659348 G A 21 GENIC homozygous 894634508 19 14659420 14659421 A G 27 GENIC homozygous 894634509 19 14659588 14659589 C T 12 GENIC homozygous 894634510 19 14660318 14660319 G A 12 GENIC homozygous 894634511 19 14661428 14661429 T A 18 GENIC homozygous 894634512 19 14662496 14662497 A G 16 GENIC homozygous 894634513 19 14662927 14662928 T C 13 GENIC homozygous 894634514 19 14663545 14663546 A G 10 GENIC homozygous 894634515 19 14663776 14663777 T C 17 GENIC homozygous 894634516