Table 1. Novel variants identified in the current study.

No.	Chr	Position	Reference	Observed	Location	Gene	Frequency	Read depth	Pool 1	Pool 2	Pool 3	Pool 4
1	Chr3	8790685	C	T	Intergenic	—	0.009	13,557	•	—	—	—
2	Chr3	8791451	C	A	Downstream	OXTR	0.022	63,594	•	•	•	•
3	Chr3	8791453	T	C	Downstream	OXTR	0.02	64,498	•	•	•	•
4	Chr3	8791455	T	C	Downstream	OXTR	0.02	64,354	•	•	•	•
5	Chr3	8793620	A	T	UTR3	OXTR	0.007	36,037	—	•	•	—
6	Chr3	8793928	T	C	UTR3	OXTR	0.017	30,415	•	•	•	•
7	Chr3	8793930	T	C	UTR3	OXTR	0.01	30,303	•	•	—	•
8	Chr3	8793950	T	A	UTR3	OXTR	0.008	30,705	—	•	—	•
9	Chr3	8794920	T	G	Intronic	OXTR	0.019	35,201	•	•	•	•
10	Chr3	8795600	G	A	Intronic	OXTR	0.008	48,582	—	•	—	—
11	Chr3	8795876	C	T	Intronic	OXTR	0.006	39,391	—	•	—	—
12	Chr3	8797707	T	C	Intronic	OXTR	0.006	47,351	—	—	—	•
13	Chr3	8798395	G	A	Intronic	OXTR	0.019	48,715	•	•	—	•
14	Chr3	8798903	T	A	Intronic	OXTR	0.01	29,912	•	•	—	•
15	Chr3	8800614	T	C	Intronic	OXTR	0.009	50,854	—	—	—	•
16	Chr3	8801278	G	A	Intronic	OXTR	0.009	46,203	—	—	—	•
17	Chr3	8802373	G	A	Intronic	OXTR	0.012	54,288	—	—	•	—
18	Chr3	8802838	T	A	Intronic	OXTR	0.005	58,478	—	—	•	—
19	Chr3	8803740	T	G	Intronic	OXTR	0.01	53,209	•	•	—	—
20	Chr3	8803900	A	C	Intronic	OXTR	0.009	44,269	•	—	—	—
21	Chr3	8805516	A	G	Intronic	OXTR	0.021	38,133	—	—	—	•
22	Chr3	8805681	A	G	Intronic	OXTR	0.009	29,916	—	—	•	—
23	Chr3	8805870	C	T	Intronic	OXTR	0.017	44,279	•	•	•	•
24	Chr3	8805871	C	T	Intronic	OXTR	0.016	44,208	•	•	•	•
25	Chr3	8805874	A	C	Intronic	OXTR	0.014	43,421	•	•	•	•
26	Chr3	8807814	A	G	Intronic	OXTR	0.008	45,546	—	—	—	•
27	Chr3	8808386	C	G	Intronic	OXTR	0.008	25,157	—	•	—	—
28	Chr3	8809426	G	T	Exonic	OXTR	0.006	31,586	—	•	—	—

The positions, single-nucleotide changes compared against reference genome, and frequencies of a total of 28 novel variants were shown. The black dot indicates that the mutation was observed in the given pool, whereas the dash indicates that the mutation was not found.

Abbreviations: Chr, chromosome; OXTR, oxytocin receptor.