chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 17183959 17183960 A G 53 GENIC homozygous 144358052 5 17184099 17184100 A G 50 GENIC homozygous 144358053 5 17185093 17185094 T C 42 GENIC homozygous 144358054 5 17185144 17185145 G T 39 GENIC homozygous 144358055 5 17185515 17185516 G A 44 GENIC homozygous 144358056 5 17185957 17185958 T A 41 GENIC homozygous 144358057 5 17186055 17186056 G A 44 GENIC homozygous 144358058 5 17186127 17186128 G A 40 GENIC possibly homozygous 144358059 5 17186618 17186619 C G 38 GENIC homozygous 137389733 5 17185322 17185323 T A 45 GENIC homozygous 137389730 5 17185988 17185989 C G 41 GENIC homozygous 137389732 5 17185623 17185624 A G 54 GENIC possibly homozygous 147538387 5 17186488 17186489 G A 47 GENIC homozygous 147538388 5 17186500 17186501 T G 45 GENIC homozygous 147538389 5 17185988 17185989 C A 41 GENIC heterozygous 403133975 5 17186722 17186723 T C 37 GENIC homozygous 144358060 5 17186947 17186948 A G 46 GENIC homozygous 137389734 5 17186952 17186953 A T 45 GENIC homozygous 137389735 5 17187616 17187617 C T 54 GENIC homozygous 147538390 5 17187763 17187764 C T 39 GENIC homozygous 147538391 5 17188009 17188010 G A 48 GENIC homozygous 147538392 5 17187419 17187420 C T 43 GENIC homozygous 144358061 5 17187924 17187925 T A 52 GENIC homozygous 144358062