chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 13310593 13310594 G C 29 GENIC homozygous 531955644 12 13311026 13311027 C G 12 GENIC homozygous 531955645 12 13311053 13311054 C CT 7 GENIC possibly homozygous 694493532 12 13312996 13312997 T G 30 GENIC homozygous 530374116 12 13313883 13313884 A G 28 GENIC homozygous 530374117 12 13313937 13313938 G A 19 GENIC homozygous 530374118 12 13315924 13315925 G A 27 GENIC possibly homozygous 530374119 12 13316022 13316025 ACA --- 11 GENIC possibly homozygous 694493534 12 13316024 13316025 A - 11 GENIC possibly homozygous 694493535 12 13316024 13316025 A AC 11 GENIC possibly homozygous 694493536 12 13316032 13316033 C - 12 GENIC heterozygous 694493537 12 13316068 13316069 C CCCCATT 11 GENIC homozygous 694493538 12 13316168 13316169 C CT 9 GENIC heterozygous 694493539 12 13316501 13316503 CC -- 17 GENIC homozygous 694493541 12 13316866 13316867 T C 19 GENIC possibly homozygous 531955646 12 13316870 13316871 A G 18 GENIC homozygous 531955647 12 13316979 13316980 C T 29 GENIC homozygous 531955648 12 13317149 13317150 G GT 19 GENIC heterozygous 694493542 12 13318452 13318465 GTTGGAGAGGAAT ------------- 10 GENIC homozygous 694493543 12 13318466 13318476 TTGGAGAGGA ---------- 12 GENIC homozygous 694493544 12 13318478 13318481 GAC --- 17 GENIC heterozygous 694493545 12 13318806 13318807 A G 15 GENIC heterozygous 531955649 12 13318931 13318932 G A 29 GENIC possibly homozygous 531955650