chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 20935703 20935704 C T 13 GENIC homozygous 791158965 14 20935965 20935966 G A 9 GENIC homozygous 791158966 14 20936350 20936351 G A 19 GENIC homozygous 791158967 14 20938336 20938337 T G 32 GENIC possibly homozygous 791158968 14 20939038 20939039 A T 21 GENIC homozygous 791158969 14 20939394 20939395 A G 22 GENIC homozygous 791158970 14 20941643 20941644 A G 7 GENIC homozygous 791158971 14 20941663 20941664 G C 5 GENIC homozygous 791158972 14 20942085 20942086 C A 12 GENIC homozygous 791158973 14 20942140 20942141 C G 14 GENIC homozygous 791158974 14 20942229 20942230 T C 13 GENIC homozygous 791158975 14 20942232 20942233 C A 13 GENIC homozygous 791158976 14 20942614 20942615 G C 21 GENIC homozygous 791158977 14 20944684 20944685 A G 15 GENIC homozygous 791158978 14 20944912 20944913 A G 26 GENIC homozygous 791158979 14 20946014 20946015 A T 16 GENIC homozygous 791158980 14 20947570 20947571 A G 17 GENIC homozygous 791158981 14 20948218 20948219 G A 18 GENIC homozygous 791158982 14 20948383 20948384 G A 18 GENIC homozygous 791158983 14 20948435 20948436 A T 14 GENIC homozygous 791158984 14 20948985 20948986 G C 23 GENIC homozygous 791158985 14 20948998 20948999 T A 29 GENIC homozygous 791158986 14 20949006 20949007 A T 26 GENIC homozygous 791158987 14 20949008 20949009 G C 26 GENIC homozygous 791158988 14 20949540 20949541 T G 23 GENIC possibly homozygous 791158989 14 20949562 20949563 A T 24 GENIC homozygous 791158990 14 20950421 20950422 C A 17 GENIC homozygous 791158991 14 20951075 20951076 C T 20 GENIC homozygous 791158992 14 20952226 20952227 C T 19 GENIC possibly homozygous 791158993