chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 20935703 20935704 C T 19 GENIC homozygous 976962809 14 20935965 20935966 G A 21 GENIC homozygous 976962810 14 20936350 20936351 G A 16 GENIC homozygous 976962811 14 20939038 20939039 A T 28 GENIC homozygous 976962812 14 20939394 20939395 A G 28 GENIC homozygous 976962813 14 20942229 20942230 T C 19 GENIC homozygous 976962814 14 20942232 20942233 C A 18 GENIC homozygous 976962815 14 20942614 20942615 G C 20 GENIC homozygous 976962816 14 20944684 20944685 A G 34 GENIC homozygous 976962817 14 20946014 20946015 A T 26 GENIC homozygous 976962818 14 20947570 20947571 A G 20 GENIC homozygous 976962819 14 20948218 20948219 G A 23 GENIC homozygous 976962820 14 20948383 20948384 G A 15 GENIC homozygous 976962821 14 20948435 20948436 A T 22 GENIC homozygous 976962822 14 20948985 20948986 G C 19 GENIC homozygous 976962823 14 20948989 20948990 T A 18 GENIC homozygous 976962824 14 20948992 20948993 G T 18 GENIC homozygous 976962825 14 20948998 20948999 T A 16 GENIC homozygous 976962826 14 20949006 20949007 A T 18 GENIC homozygous 976962827 14 20949008 20949009 G C 18 GENIC homozygous 976962828 14 20949540 20949541 T G 17 GENIC possibly homozygous 976962829 14 20949562 20949563 A T 23 GENIC homozygous 976962830 14 20950421 20950422 C A 20 GENIC homozygous 976962831 14 20951075 20951076 C T 36 GENIC homozygous 976962832 14 20952226 20952227 C T 13 GENIC homozygous 976962833