chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 125743344 125743345 A T 4 GENIC heterozygous 597607890 7 125743354 125743355 C A 4 GENIC heterozygous 597607891 7 125744815 125744816 G A 15 GENIC possibly homozygous 597607892 7 125747094 125747095 C T 22 GENIC heterozygous 597097186 7 125747095 125747096 C T 21 GENIC heterozygous 597097187 7 125747420 125747421 G A 29 GENIC homozygous 597097188 7 125747534 125747535 C T 24 GENIC possibly homozygous 597097189 7 125747647 125747655 CAACATGA -------- 3 GENIC heterozygous 727207793 7 125747681 125747682 T G 16 GENIC possibly homozygous 597097190 7 125747731 125747733 TG -- 19 GENIC homozygous 727207794 7 125748235 125748236 T C 25 GENIC possibly homozygous 597097191 7 125748533 125748534 T C 31 GENIC possibly homozygous 597607893 7 125748640 125748641 C G 3 GENIC heterozygous 597097192 7 125748927 125748928 G A 29 GENIC homozygous 597097193 7 125749414 125749415 A G 18 GENIC homozygous 597097194 7 125749577 125749578 G GGCAGTCAGTGCCC 3 GENIC homozygous 727207795 7 125749657 125749658 G T 21 GENIC homozygous 597607894 7 125751261 125751262 G A 23 GENIC possibly homozygous 597607895 7 125752000 125752001 T C 21 GENIC homozygous 597097195 7 125753897 125753898 C T 5 GENIC homozygous 597097196 7 125753949 125753950 G A 10 GENIC homozygous 597097197 7 125754274 125754275 A G 27 GENIC homozygous 597097198 7 125754320 125754321 C T 11 GENIC homozygous 597097199 7 125754367 125754368 C T 15 GENIC possibly homozygous 597097200 7 125754379 125754380 G C 12 GENIC homozygous 597097201 7 125755157 125755158 G A 8 GENIC heterozygous 597097202 7 125755666 125755667 C T 15 GENIC possibly homozygous 597097203 7 125755703 125755704 C T 24 GENIC homozygous 597097204 7 125756500 125756501 T C 17 GENIC homozygous 597097205 7 125756849 125756850 A G 12 GENIC heterozygous 597097206 7 125757153 125757154 T TA 1 GENIC homozygous 727207796