chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 85733189 85733190 C T 29 GENIC possibly homozygous 66544752 14 85733664 85733665 C T 45 GENIC homozygous 66986982 14 85734666 85734667 T C 43 GENIC homozygous 66986984 14 85735100 85735101 A G 49 GENIC homozygous 66544754 14 85736561 85736562 T A 47 GENIC homozygous 67090763 14 85737552 85737553 C A 30 GENIC homozygous 66986986 14 85743805 85743806 A C 37 GENIC homozygous 66544758 14 85745251 85745252 A C 29 GENIC homozygous 67513933 14 85745256 85745257 A G 28 GENIC homozygous 66544760 14 85745264 85745265 C T 31 GENIC homozygous 66544761 14 85745573 85745574 T C 52 GENIC homozygous 66986990 14 85748271 85748272 C G 40 GENIC homozygous 66544764 14 85748755 85748756 A G 54 GENIC homozygous 66544765 14 85736791 85736792 T C 40 GENIC homozygous 66646697 14 85742066 85742067 G A 30 GENIC heterozygous 67588170 14 85745081 85745082 G A 24 GENIC possibly homozygous 67588171 14 85749382 85749383 G T 53 GENIC homozygous 66106653 14 85751864 85751865 A G 23 GENIC homozygous 66106655 14 85752241 85752242 C T 20 GENIC homozygous 67588172 14 85753474 85753475 G A 51 GENIC homozygous 66987004 14 85754014 85754015 T C 55 GENIC homozygous 66544767 14 85754463 85754464 T C 41 GENIC homozygous 66987006 14 85754492 85754493 T C 38 GENIC homozygous 66987008 14 85754510 85754511 T C 46 GENIC homozygous 67090775 14 85754652 85754653 C T 30 GENIC homozygous 66987010 14 85755117 85755118 G A 31 GENIC homozygous 66987012 14 85755120 85755121 G A 33 GENIC homozygous 66646699 14 85756951 85756952 A G 47 GENIC homozygous 66987016 14 85757935 85757936 C T 38 GENIC homozygous 66544769 14 85758494 85758495 C G 29 GENIC possibly homozygous 66646703 14 85758623 85758624 G C 33 GENIC homozygous 66544771