chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 60004343 60004344 T C 22 GENIC homozygous 51466694 10 60004414 60004415 A T 23 GENIC homozygous 51466695 10 60004474 60004475 G A 21 GENIC homozygous 51466696 10 60004710 60004711 C T 20 GENIC homozygous 51466697 10 60004951 60004952 C A 9 GENIC homozygous 51466698 10 60005008 60005009 G A 11 GENIC homozygous 51466699 10 60005162 60005163 C T 11 GENIC homozygous 51466700 10 60005212 60005213 G A 12 GENIC possibly homozygous 51466701 10 60005219 60005220 G A 11 GENIC homozygous 51466702 10 60005412 60005413 C G 15 GENIC homozygous 51466703 10 60006307 60006308 C G 17 GENIC homozygous 51466716 10 60006334 60006335 G A 21 GENIC homozygous 51466717 10 60006434 60006435 G A 30 GENIC homozygous 51466718 10 60006551 60006552 T A 19 GENIC homozygous 51466720 10 60006987 60006988 G A 32 GENIC homozygous 51466723 10 60007199 60007200 T C 25 GENIC possibly homozygous 51466725 10 60007550 60007551 T C 11 GENIC homozygous 51466731 10 60007928 60007930 AG -- 7 GENIC possibly homozygous 51466735 10 60008639 60008640 T A 22 GENIC homozygous 51466742 10 60009107 60009108 C A 9 GENIC homozygous 51466746 10 60009451 60009452 A G 11 GENIC homozygous 51466748 10 60009797 60009798 T TA 21 GENIC homozygous 51466749 10 60011176 60011177 A C 23 GENIC homozygous 51466750 10 60011264 60011265 A G 23 GENIC homozygous 51466751 10 60011642 60011643 C T 19 GENIC homozygous 51466752 10 60011841 60011842 A AG 23 GENIC homozygous 51466753 10 60011857 60011858 A - 23 GENIC homozygous 51466754 10 60012002 60012003 G A 29 GENIC homozygous 51466755