chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 6611288 6611289 G GT 18 GENIC homozygous 737000204 20 6611372 6611373 A G 28 GENIC homozygous 615129640 20 6611464 6611465 A T 24 GENIC homozygous 614416304 20 6611465 6611466 A C 24 GENIC homozygous 614416305 20 6611597 6611602 TTTCG ----- 22 GENIC homozygous 737000205 20 6611688 6611689 T C 24 GENIC homozygous 614416306 20 6612400 6612401 G C 19 GENIC homozygous 614416307 20 6612770 6612771 G A 34 GENIC homozygous 614416308 20 6612996 6612997 C T 31 GENIC homozygous 614416309 20 6613051 6613052 A C 22 GENIC homozygous 614416310 20 6613073 6613080 AAAAAAC ------- 24 GENIC possibly homozygous 737000206 20 6613120 6613121 A G 39 GENIC homozygous 614416311 20 6613534 6613535 C A 26 GENIC homozygous 614416312 20 6613555 6613556 A G 21 GENIC homozygous 614416313 20 6614651 6614652 C T 29 GENIC homozygous 614416314 20 6614840 6614844 ATTT ---- 11 GENIC homozygous 737000207 20 6614953 6614954 C A 1 GENIC homozygous 615129641 20 6615189 6615190 C - 27 GENIC homozygous 737000208 20 6615265 6615266 A G 28 GENIC homozygous 614416315 20 6615381 6615382 G A 30 GENIC homozygous 614416316 20 6615453 6615454 C CA 34 GENIC homozygous 737000209