TABLE 3.

Information of six genomic variations.

Chr	Start	Ref	Alt	Location	Gene.refGene	Modification types
chr5	118605129	ATG	A	Intronic	TNFAIP8	H3K4me3
chr5	88179358	A	G	ncRNA_intronic	MEF2C	H3K4me3
chr17	62339443	G	T	Intronic	TEX2	H3K4me3
chr7	41740828	G	A	ncRNA_intronic	INHBA-AS1	H3K4me3
chr1	20811135	T	C	Intronic	CAMK2N1	H3K4me3
chr7	94023911	A	G	UTR5	COL1A2	H3K27ac

Column Location lists the genomic region of the variation. ncRNA_intronic means non-coding RNA genes. Gene.refGene is the gene associating the variation. Modification types indicate the H3K4me3 or H3K27ac around the variation in both H1 and H1_BMP4.