chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 24103800 24103801 T G 9 GENIC homozygous 962110549 14 24103859 24103860 T A 16 GENIC homozygous 962110550 14 24104271 24104272 T C 29 GENIC homozygous 962110551 14 24104367 24104368 T C 24 GENIC homozygous 962110552 14 24104416 24104417 G C 19 GENIC homozygous 962110553 14 24104564 24104565 G A 22 GENIC homozygous 962110554 14 24104718 24104719 G A 23 GENIC homozygous 962110555 14 24104742 24104743 T C 24 GENIC homozygous 962110556 14 24109614 24109615 T C 21 GENIC homozygous 962110557 14 24109642 24109643 C T 20 GENIC homozygous 962110558 14 24109823 24109824 G T 27 GENIC homozygous 962110559 14 24109894 24109895 G T 23 GENIC homozygous 962110560 14 24109990 24109991 G C 24 GENIC homozygous 962110561 14 24116090 24116091 C G 13 GENIC homozygous 962110562 14 24116537 24116538 T C 23 GENIC homozygous 962110563 14 24116710 24116711 G A 19 GENIC homozygous 962110564 14 24117045 24117046 A C 25 GENIC homozygous 962110565 14 24119438 24119439 T A 32 GENIC homozygous 962110566 14 24119888 24119889 G A 21 GENIC homozygous 962110567 14 24121237 24121238 G A 17 GENIC homozygous 962110568 14 24121487 24121488 G A 18 GENIC homozygous 962110569 14 24121869 24121870 A T 30 GENIC homozygous 962110570 14 24123292 24123293 G T 23 GENIC homozygous 962110571 14 24123313 24123314 G C 18 GENIC homozygous 962110572 14 24123891 24123892 G C 18 GENIC homozygous 962110573 14 24124628 24124629 A G 10 GENIC homozygous 962110574 14 24125242 24125243 T C 28 GENIC homozygous 962110575