Table 3. Sequencing and mapping summary.

	F_2010_1	C2*	C4*
Total reads	686,558,582	1,081,810,248	989,568,234
Passed reads	652,488,758	632,750,570	845,549,706
Mapped/passed reads	95.04%	99.56%	99.38%
Reads after duplicate reads removed	595,705,705	625,962,801	723,928,404
Coverage >=1	99.20%	97.30%	97.40%
Coverage >=10	97.50%	95.20%	97.10%
Coverage >=30	64.50%	64.20%	82.80%
Average depth >=1	35.90%	38.70%	44.60%
Average depth >=10	36.40%	39.40%	44.80%
Average depth >=30	42.50%	47.90%	48.20%
Identified SNPs	6,064,956	-	-
Identified INDELs	727,565	-	-

SNPs, single nucleotide polymorphisms; INDELs, insertions/deletions. *Tozaki et al. 2020 [23].