chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 60620465 60620466 T C 13 GENIC homozygous 983822609 18 60620603 60620604 T C 16 GENIC homozygous 983822610 18 60621346 60621347 G A 22 GENIC homozygous 983822611 18 60624249 60624250 G A 32 GENIC homozygous 983822612 18 60624297 60624298 T A 33 GENIC homozygous 983822613 18 60624298 60624299 A T 33 GENIC homozygous 983822614 18 60625800 60625801 T C 16 GENIC homozygous 983822615 18 60626242 60626243 A T 13 GENIC homozygous 983822616 18 60626632 60626633 T C 20 GENIC homozygous 983822617 18 60626871 60626872 C T 28 GENIC homozygous 983822618 18 60627484 60627485 T C 27 GENIC homozygous 983822619 18 60628800 60628801 A G 14 GENIC homozygous 983822620 18 60631251 60631252 C T 23 GENIC homozygous 983822621 18 60631509 60631510 G A 27 GENIC homozygous 983822622