chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 37564004 37564005 C A 22 GENIC homozygous 970621561 12 37564549 37564550 T C 34 GENIC homozygous 970621562 12 37564784 37564785 T C 31 GENIC homozygous 970621563 12 37567045 37567046 T C 29 GENIC homozygous 970621564 12 37567276 37567277 A C 26 GENIC homozygous 970621565 12 37567397 37567398 T C 21 GENIC homozygous 970621566 12 37567898 37567899 C T 33 GENIC homozygous 970621567 12 37567939 37567940 A C 38 GENIC homozygous 970621568 12 37569481 37569482 C G 34 GENIC homozygous 970621569 12 37569732 37569733 G A 35 GENIC homozygous 970621570 12 37570869 37570870 G A 39 GENIC homozygous 970621571 12 37571673 37571674 A G 28 GENIC homozygous 970621572 12 37572327 37572328 G A 30 GENIC homozygous 970621573 12 37574609 37574610 C A 28 GENIC homozygous 970621574 12 37574610 37574611 T G 28 GENIC homozygous 970621575 12 37574619 37574620 A G 28 GENIC homozygous 970621576 12 37574633 37574634 C G 24 GENIC homozygous 970621577 12 37577303 37577304 G T 18 GENIC homozygous 970621578 12 37578538 37578539 G A 24 GENIC homozygous 970621579 12 37578715 37578716 C A 35 GENIC possibly homozygous 970621580 12 37579482 37579483 T C 30 GENIC homozygous 970621581 12 37579916 37579917 G T 13 GENIC homozygous 970621582 12 37579917 37579918 A G 14 GENIC homozygous 970621583 12 37579958 37579959 C T 19 GENIC homozygous 970621584