chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 4232726 4232727 A G 6 GENIC homozygous 554304099 12 4233335 4233336 G A 24 GENIC homozygous 555183961 12 4233661 4233662 A AGTGTGTGTGTGTGTGT 5 GENIC homozygous 701696142 12 4233769 4233771 GT -- 14 GENIC homozygous 701696143 12 4233888 4233889 G A 30 GENIC homozygous 554304100 12 4234088 4234089 T C 22 GENIC homozygous 554304101 12 4234305 4234306 T C 28 GENIC homozygous 554304102 12 4234661 4234666 ACACA ----- 4 GENIC heterozygous 701696145 12 4234661 4234664 ACA --- 4 GENIC heterozygous 701696146 12 4235434 4235435 C T 35 GENIC possibly homozygous 555183962 12 4235583 4235615 CACACAGACACACCTACATACACAGACACACT -------------------------------- 24 GENIC homozygous 701696147 12 4235927 4235928 T C 27 GENIC homozygous 554304103 12 4235985 4235986 T C 42 GENIC homozygous 554304104 12 4237412 4237413 T TGGTTATTCAACTCGACCTTTGAA 25 GENIC homozygous 701696148 12 4237445 4237446 A AT 28 GENIC homozygous 701696149 12 4237452 4237453 G A 28 GENIC homozygous 554304105 12 4237706 4237709 AGT --- 21 GENIC homozygous 701696150 12 4237816 4237817 C T 18 GENIC homozygous 554304106 12 4237892 4237893 A G 23 GENIC homozygous 554304107 12 4238950 4238951 C T 25 GENIC homozygous 555183963 12 4240150 4240151 C CT 10 GENIC homozygous 701696151 12 4244034 4244035 T TTCTCTCTCTCTC 6 GENIC heterozygous 701696156 12 4244083 4244089 GTGTGT ------ 13 GENIC homozygous 701696157 12 4244303 4244304 G A 31 GENIC homozygous 555183964 12 4245429 4245430 G GAC 34 GENIC possibly homozygous 701696163 12 4245605 4245642 GCACACAGCACACATACACACACACGCACACATACAC ------------------------------------- 25 GENIC homozygous 701696164 12 4246574 4246575 C G 25 GENIC possibly homozygous 554304108 12 4249190 4249191 G - 8 GENIC heterozygous 701696165 12 4254705 4254709 TACA ---- 25 GENIC homozygous 701696167 12 4256999 4257000 G A 11 GENIC homozygous 554304109 12 4259306 4259307 G A 25 GENIC homozygous 554304110 12 4260298 4260299 C T 18 GENIC homozygous 554304111