TABLE 1.

Primers used in this study

F, forward; R, reverse; LK, linker.

	5′ to 3′
Primers for ChIP PCRs
Promoter F	CCCCACATACCCAACTGCTG
Promoter R	GCCCGCCGCTTCTAAAATTC
Exon 1 3′ end F	AGCAGCATGTGGACTCTC
Exon 1 R2	TGGGCTGGGCTGGGTGACGCCAGG
Up GAA F	GAAACCCAAAGAATGGCTGTG
Up GAA R	TTCCCTCCTCGTGAAACACC
Down GAA F	CTGGAAAAATAGGCAAGTGTGG
Down GAA R	CAGGGGTGGAAGCCCAATAC
Exon 2 F	GCCTCAACCAGATTTGGAAT
Exon 2 R	GCCCAAAGTTCCAGATTT
GAPDH exon 1 F	TCGACAGTCAGCCGCATCT
GAPDH intron 1 R	CTAGCCTCCCGGGTTTCTCT
MYO-D exon 1 F	CCGCCTGAGCAAAGTAAATGA
MYO-D exon 1 R	GGCAACCGCTGGTTTGG
Primers for reverse transcription
LK exon 1 3′ end	actggagcacgaggacactCAGGTCGCATCGATGTC
LK exon 2	actggagcacgaggacactGCCCAAAGTTCCAGATTT
Exon 1 R2	TGGGCTGGGCTGGGTGACGCCAGG
Primers for SYBR Green PCR
LK primer	ACTGGAGCACGAGGACACT
Exon 3 F	CAGAGGAAACGCTGGACTCT
Exon 4 R	AGCCAGATTTGCTTGTTTGG
GUS F	CTCATTTGGAATTTTGCCGATT
GUS R	CCGAGTGAAGATCCCCTTTTTA
Exon 2 F	GCCTCAACCAGATTTGGAAT
Exon 1 3′ end F	AGCAGCATGTGGACTCTC