chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 10741444 10741445 T C 39 GENIC possibly homozygous 809691855 17 10741502 10741503 A G 42 GENIC possibly homozygous 809691856 17 10742269 10742270 A G 58 GENIC homozygous 809691857 17 10742613 10742614 C T 38 GENIC homozygous 809691858 17 10743548 10743549 A T 33 GENIC homozygous 809691859 17 10743861 10743862 C T 33 GENIC homozygous 809691860 17 10743946 10743947 A G 33 GENIC homozygous 809691861 17 10744694 10744695 T G 53 GENIC homozygous 809691862 17 10744844 10744845 T A 46 GENIC homozygous 809691863 17 10745781 10745782 T G 64 GENIC possibly homozygous 809691864 17 10746039 10746040 G C 44 GENIC homozygous 809691865 17 10746047 10746048 G A 41 GENIC possibly homozygous 809691866 17 10760680 10760681 T C 39 GENIC homozygous 809691867 17 10761275 10761276 A T 41 GENIC homozygous 809691868 17 10767606 10767607 C G 59 GENIC heterozygous 809691869 17 10768419 10768420 C G 38 GENIC homozygous 809691870 17 10769187 10769188 T G 34 GENIC possibly homozygous 809691871