chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 14654618 14654619 C T 18 GENIC homozygous 951233027 19 14654824 14654825 G A 13 GENIC homozygous 951233028 19 14654826 14654827 G A 10 GENIC homozygous 951233029 19 14655942 14655943 C T 12 GENIC homozygous 951233030 19 14656129 14656130 C T 6 GENIC homozygous 951233031 19 14656676 14656677 G A 13 GENIC homozygous 951233032 19 14657553 14657554 A G 14 GENIC homozygous 951233033 19 14657578 14657579 C T 15 GENIC homozygous 951233034 19 14658363 14658364 T C 14 GENIC homozygous 951233035 19 14659257 14659258 C T 12 GENIC homozygous 951233036 19 14659347 14659348 G A 6 GENIC homozygous 951233037 19 14659420 14659421 A G 12 GENIC homozygous 951233038 19 14659588 14659589 C T 15 GENIC homozygous 951233039 19 14660318 14660319 G A 8 GENIC homozygous 951233040 19 14661428 14661429 T A 17 GENIC homozygous 951233041 19 14662496 14662497 A G 9 GENIC homozygous 951233042 19 14663545 14663546 A G 7 GENIC homozygous 951233043 19 14663776 14663777 T C 10 GENIC homozygous 951233044