chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 87431062 87431063 G A 21 GENIC homozygous 116899815 10 87431142 87431143 A C 25 GENIC homozygous 116899817 10 87432056 87432057 C T 27 GENIC homozygous 116899823 10 87432078 87432079 A G 27 GENIC homozygous 116899825 10 87432522 87432523 C G 32 GENIC homozygous 117152370 10 87432606 87432607 C T 30 GENIC homozygous 116899829 10 87433162 87433163 C G 14 GENIC homozygous 117152371 10 87433212 87433213 T C 16 GENIC homozygous 117152372 10 87433219 87433220 T C 19 GENIC homozygous 117152373 10 87433723 87433724 A G 27 GENIC homozygous 116899833 10 87433843 87433844 A G 34 GENIC homozygous 116899835 10 87433962 87433963 C A 30 GENIC homozygous 116899837 10 87433990 87433991 C G 29 GENIC homozygous 116899839 10 87434118 87434119 G A 27 GENIC homozygous 117152374 10 87434259 87434260 C T 33 GENIC homozygous 117152375 10 87434993 87434994 C A 23 GENIC homozygous 117152376 10 87435046 87435047 C T 29 GENIC homozygous 117152377 10 87435111 87435112 C T 35 GENIC homozygous 117152378 10 87435405 87435406 T C 30 GENIC homozygous 117179991 10 87435406 87435407 G A 30 GENIC homozygous 117152379 10 87435570 87435571 G C 29 GENIC homozygous 117152380 10 87436261 87436262 G C 25 GENIC homozygous 117152381 10 87436288 87436289 C T 19 GENIC homozygous 117152382 10 87436369 87436370 A G 21 GENIC homozygous 117152383