chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 14653806 14653807 G A 20 GENIC homozygous 974247995 19 14654618 14654619 C T 22 GENIC homozygous 974247996 19 14654824 14654825 G A 28 GENIC homozygous 974247997 19 14654826 14654827 G A 29 GENIC homozygous 974247998 19 14656129 14656130 C T 28 GENIC homozygous 974247999 19 14656676 14656677 G A 33 GENIC homozygous 974248000 19 14657553 14657554 A G 26 GENIC homozygous 974248001 19 14657578 14657579 C T 28 GENIC homozygous 974248002 19 14658363 14658364 T C 20 GENIC homozygous 974248003 19 14659257 14659258 C T 30 GENIC homozygous 974248004 19 14659347 14659348 G A 29 GENIC homozygous 974248005 19 14659420 14659421 A G 37 GENIC homozygous 974248006 19 14659588 14659589 C T 29 GENIC homozygous 974248007 19 14660318 14660319 G A 38 GENIC homozygous 974248008 19 14661428 14661429 T A 30 GENIC homozygous 974248009 19 14662496 14662497 A G 29 GENIC homozygous 974248010 19 14662927 14662928 T C 26 GENIC homozygous 974248011 19 14663545 14663546 A G 22 GENIC homozygous 974248012