chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 60619766 60619767 T G 21 GENIC possibly homozygous 814389605 18 60620465 60620466 T C 25 GENIC homozygous 814389606 18 60620603 60620604 T C 33 GENIC homozygous 814389607 18 60621346 60621347 G A 37 GENIC homozygous 814389608 18 60623296 60623297 T C 42 GENIC heterozygous 814389609 18 60624249 60624250 G A 26 GENIC homozygous 814389610 18 60625800 60625801 T C 29 GENIC homozygous 814389611 18 60626242 60626243 A T 43 GENIC homozygous 814389612 18 60626632 60626633 T C 19 GENIC homozygous 814389613 18 60626871 60626872 C T 33 GENIC homozygous 814389614 18 60627484 60627485 T C 24 GENIC homozygous 814389615 18 60628800 60628801 A G 29 GENIC homozygous 814389616 18 60631251 60631252 C T 41 GENIC homozygous 814389617 18 60631509 60631510 G A 21 GENIC homozygous 814389618