chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 104195752 104195753 C A 10 GENIC homozygous 108735625 1 104195755 104195761 CCCCCC 10 GENIC homozygous 127409404 1 104198136 104198137 C 5 GENIC homozygous 127409405 1 104198705 104198706 C A 16 GENIC homozygous 108165709 1 104198716 104198718 CT 19 GENIC homozygous 127409410 1 104198732 104198733 A 22 GENIC homozygous 127409411 1 104198849 104198850 G 27 GENIC homozygous 127409412 1 104200493 104200493 AAATTCATCTCCAGATAAGT 39 GENIC possibly homozygous 127409413 1 104200497 104200497 CTGCAGAGGAAAAGGTAAACAGT 28 GENIC homozygous 127409414 1 104200500 104200500 TCG 29 GENIC homozygous 127409415 1 104200503 104200503 TGAAACAAA 20 GENIC homozygous 127409416 1 104200506 104200506 TGACAGATTTACCGGGGGGCATC 18 GENIC homozygous 127409417 1 104200512 104200512 AGATGACTAAC 16 GENIC homozygous 127409418 1 104200516 104200516 CTTACCCACACGTACACACGGTTTGAACAGC 15 GENIC homozygous 127409419 1 104200519 104200519 AACAAA 17 GENIC homozygous 127409420 1 104201321 104201322 C G 49 GENIC homozygous 108165710 1 104201340 104201341 C A 50 GENIC homozygous 108165711 1 104200510 104200511 G C 16 GENIC homozygous 127546319