chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 106480929 106480930 C G 51 GENIC homozygous 146263920 13 106481037 106481038 A T 56 GENIC homozygous 146263921 13 106482444 106482445 A G 54 GENIC homozygous 139371534 13 106483758 106483759 A G 61 GENIC possibly homozygous 139371536 13 106483844 106483845 T C 59 GENIC possibly homozygous 139371537 13 106484181 106484182 A G 69 GENIC homozygous 139371539 13 106484393 106484394 G A 65 GENIC homozygous 146263922 13 106484417 106484418 G A 64 GENIC homozygous 146263923 13 106484422 106484423 T C 66 GENIC homozygous 139371540 13 106487342 106487343 A G 60 GENIC homozygous 146263924 13 106487694 106487695 T C 58 GENIC possibly homozygous 143597150 13 106487820 106487821 C G 45 GENIC homozygous 139371541 13 106487863 106487864 G C 52 GENIC homozygous 146263925 13 106488178 106488179 A G 60 GENIC homozygous 146263926 13 106488349 106488350 T C 47 GENIC homozygous 139371542 13 106488892 106488893 A G 55 GENIC homozygous 139371543 13 106489013 106489014 G T 46 GENIC homozygous 146263927 13 106489781 106489782 A G 64 GENIC homozygous 139371544 13 106489888 106489889 T C 57 GENIC homozygous 139371545 13 106482798 106482799 A 57 GENIC possibly homozygous 141096281 13 106484773 106484791 CCTCTCCCTCTTCCTCTT 46 GENIC homozygous 146259643 13 106487879 106487884 CCAGG 48 GENIC homozygous 146259644 13 106494425 106494426 T 64 GENIC homozygous 139192225 13 106493393 106493402 ATTAGGAAC 58 GENIC possibly homozygous 139192224