chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 224572733 224572734 C T 24 GENIC homozygous 528870142 4 224573209 224573210 T C 17 GENIC homozygous 528870143 4 224573259 224573261 TG -- 13 GENIC homozygous 693901729 4 224573304 224573305 T G 10 GENIC homozygous 528870144 4 224573813 224573814 T - 11 GENIC heterozygous 693901730 4 224573816 224573817 T TCC 17 GENIC possibly homozygous 693901731 4 224573817 224573818 T TC 19 GENIC possibly homozygous 693901732 4 224574455 224574456 T C 27 GENIC homozygous 528870145 4 224575209 224575210 T C 11 GENIC homozygous 528870146 4 224575442 224575443 T - 15 GENIC homozygous 693901733 4 224575578 224575579 A G 11 GENIC possibly homozygous 532095125 4 224575699 224575700 G GA 5 GENIC homozygous 693901734 4 224575703 224575704 C CTTATGAGTGT 2 GENIC homozygous 693901735 4 224576326 224576327 A C 25 GENIC homozygous 528870147 4 224576402 224576403 G A 23 GENIC homozygous 528870148 4 224576561 224576562 T G 24 GENIC homozygous 528870149 4 224576594 224576595 A T 24 GENIC homozygous 528870150 4 224576851 224576852 A G 25 GENIC homozygous 528870151 4 224577057 224577058 C CA 11 GENIC homozygous 693901736 4 224577254 224577255 A G 16 GENIC homozygous 528870152 4 224577762 224577766 ACAG ---- 19 GENIC homozygous 693901737 4 224578284 224578285 A - 16 GENIC homozygous 693901738 4 224578306 224578307 A AAG 19 GENIC homozygous 693901739 4 224578387 224578388 A G 32 GENIC homozygous 528870153 4 224579979 224579980 T TG 5 GENIC homozygous 693901740 4 224580805 224580806 G C 19 GENIC homozygous 528870154