chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 86649542 86649543 T C 14 GENIC homozygous 821498588 3 86650158 86650159 T G 13 GENIC homozygous 821498589 3 86650446 86650447 A G 13 GENIC homozygous 821498590 3 86652641 86652642 A G 10 GENIC homozygous 821498591 3 86652700 86652701 A G 11 GENIC homozygous 821498592 3 86654204 86654205 T C 15 GENIC homozygous 821498593 3 86657171 86657172 T TGTGC 12 GENIC homozygous 821498594 3 86657541 86657542 C T 15 GENIC homozygous 821498595 3 86657553 86657554 C T 14 GENIC homozygous 821498596 3 86657749 86657750 T TTCC 14 GENIC homozygous 821498597 3 86658316 86658317 C G 8 GENIC heterozygous 821498598 3 86658322 86658323 C G 11 GENIC heterozygous 821498599 3 86659886 86659887 G C 14 GENIC homozygous 821498600 3 86659992 86659993 G A 8 GENIC homozygous 821498601 3 86660136 86660137 T C 9 GENIC homozygous 821498602 3 86660775 86660776 G A 16 GENIC homozygous 821498603 3 86661046 86661049 AAA --- 8 GENIC homozygous 821498604 3 86661398 86661399 C T 8 GENIC homozygous 821498605 3 86662301 86662303 GG -- 7 GENIC homozygous 821498606 3 86664060 86664061 A AAGACG 9 GENIC homozygous 821498607