chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 116823142 116823143 T C 16 GENIC homozygous 822793377 7 116823521 116823522 T C 17 GENIC homozygous 822793378 7 116824211 116824212 T C 9 GENIC homozygous 822793379 7 116825093 116825094 G A 23 GENIC homozygous 822793380 7 116825103 116825104 G A 23 GENIC homozygous 822793381 7 116825628 116825629 A T 11 GENIC homozygous 822793382 7 116826982 116826983 G A 13 GENIC homozygous 822793383 7 116828351 116828352 G T 18 GENIC homozygous 822793384 7 116829856 116829857 G T 20 GENIC homozygous 822793385 7 116832075 116832076 C CCTG 18 GENIC homozygous 822793386 7 116832310 116832311 T G 20 GENIC homozygous 822793387 7 116832608 116832611 AAA --- 18 GENIC homozygous 822793388 7 116833888 116833889 T C 24 GENIC homozygous 822793389 7 116834093 116834094 A G 11 GENIC homozygous 822793390 7 116834099 116834100 T A 11 GENIC homozygous 822793391 7 116834100 116834101 C A 11 GENIC homozygous 822793392 7 116834256 116834257 A - 12 GENIC homozygous 822793393 7 116834291 116834292 C A 11 GENIC homozygous 822793394 7 116834292 116834293 T G 11 GENIC homozygous 822793395