chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 13391624 13391625 G A 36 GENIC homozygous 970588263 12 13391841 13391842 G C 40 GENIC homozygous 970588264 12 13392220 13392221 G A 35 GENIC homozygous 970588265 12 13392954 13392955 A G 34 GENIC homozygous 970588266 12 13393106 13393107 A G 53 GENIC homozygous 970588267 12 13393184 13393185 T G 38 GENIC homozygous 970588268 12 13393314 13393315 C T 37 GENIC homozygous 970588269 12 13393368 13393369 T C 43 GENIC homozygous 970588270 12 13393663 13393664 C T 41 GENIC homozygous 970588271 12 13396627 13396628 C T 31 GENIC homozygous 970588272 12 13396937 13396938 T G 45 GENIC homozygous 970588273 12 13397272 13397273 T C 31 GENIC homozygous 970588274 12 13397500 13397501 A G 30 GENIC homozygous 970588275 12 13397797 13397798 G A 33 GENIC homozygous 970588276 12 13398140 13398141 C T 19 GENIC homozygous 970588277