chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 89722942 89722943 G C 15 GENIC homozygous 52395028 10 89723105 89723106 G GA 15 GENIC possibly homozygous 52395030 10 89723175 89723176 T C 26 GENIC homozygous 51734212 10 89724273 89724274 C CAAAAAAAAA 1 GENIC homozygous 52395032 10 89724868 89724869 C CGT 23 GENIC heterozygous 51734222 10 89724868 89724869 C CGTGT 23 GENIC possibly homozygous 52395034 10 89725102 89725103 G GA 28 GENIC possibly homozygous 52395036 10 89725588 89725590 AA -- 11 GENIC heterozygous 52395037 10 89725625 89725626 G A 24 GENIC homozygous 52395039 10 89726334 89726346 AATCAATCAATC ------------ 14 GENIC heterozygous 51734232 10 89726342 89726346 AATC ---- 14 GENIC possibly homozygous 52395041 10 89726843 89726844 C CTG 11 GENIC heterozygous 52395043 10 89726843 89726844 C CTGTG 11 GENIC heterozygous 52395045 10 89726993 89726994 A ATG 48 GENIC homozygous 52395047 10 89729426 89729427 A T 21 GENIC homozygous 51734270 10 89729562 89729563 C G 30 GENIC homozygous 52395049 10 89732278 89732279 A G 20 GENIC homozygous 52395053 10 89733404 89733405 A G 33 GENIC homozygous 52395055 10 89733466 89733467 C T 27 GENIC homozygous 52395057 10 89744004 89744005 C T 19 GENIC homozygous 52395060 10 89744602 89744603 A G 31 GENIC homozygous 51734316 10 89744675 89744679 GTGT ---- 3 GENIC heterozygous 52395062 10 89744767 89744768 C - 36 GENIC homozygous 52395064 10 89745495 89745496 G A 22 GENIC homozygous 51734320 10 89745546 89745547 A G 38 GENIC homozygous 51734322 10 89745888 89745889 C T 40 GENIC homozygous 52395066 10 89746237 89746238 T C 17 GENIC homozygous 51734326 10 89747575 89747576 T C 26 GENIC homozygous 51734328 10 89748217 89748220 AAC --- 15 GENIC homozygous 52395070