EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

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EnhancerAtlas ID
HS139-27105 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr19:46931250-46932420 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ATF3MA0605.2chr19:46932184-46932196GGTGACGTCACC+6.22
ATF3MA0605.2chr19:46932184-46932196GGTGACGTCACC-6.22
CREB1MA0018.3chr19:46932184-46932196GGTGACGTCACC+7.22
CREB1MA0018.3chr19:46932184-46932196GGTGACGTCACC-7.22
RFX1MA0509.2chr19:46932221-46932237GGTCTCCATGGCAACC-6.14
RFX1MA0509.2chr19:46932221-46932237GGTCTCCATGGCAACC+6.16
RFX2MA0600.2chr19:46932221-46932237GGTCTCCATGGCAACC+6.43
RFX2MA0600.2chr19:46932221-46932237GGTCTCCATGGCAACC-6.61
RFX5MA0510.2chr19:46932221-46932237GGTCTCCATGGCAACC+6.15
RFX5MA0510.2chr19:46932221-46932237GGTCTCCATGGCAACC-6.26
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194693180046932400
Number: 1             
IDChromosomeStartEnd
GH19I046428chr194693157446932438
Enhancer Sequence
CACCGTCCTG CCCTCGCTCT GCAGAAAGAG GTTCAGCTTG GTCAGGAATT CAATGTCCTG 60
CTTCCGGGGC ATGTAGACCA CTCTCCACAC ACCGCCCTTG CCCTTGATCT CCCTGGGGAC 120
CACGGCGTAA TTGATGTCCT CCGTCAGCTG AATGATGGCC GCCTTGGATT TATCTTCTTC 180
CAGATAGGCC TTCCCAGCCA CTTCGAACTT GCCTAGAGGT TTGAGGGGCA GCCGAATAAT 240
CTCTTCGAAT TCCTCGTGGT TGCAGTCCTC CGGGATCCCC AGGATCATCA GGGACTTGTA 300
ACTGTCCACC TCCAGGGCCT TGCACCCGTG CTCCAACAGT GCAATGTCCT TCACCCCGAA 360
CAGCATCTTG CCCAACTCTT TGAGGCAGCA GTATGCCCGC TGGTGGACAC CTGAGCTGCC 420
TCGGGAATCC ACGAAATTAT CCAGGATGCC GCGATTCCTT CCCAAAGGCT ACGAGAGAGT 480
GAGGCCTCAG GGGCCGGAGG CCGCTCCCAG GACCCCTTCG TCCAGCTCAG TGAAGGATGC 540
CCCCAGCCCC TGCCTGCAGG GCTGTGCAAC GTCGGGGCTT CTGTGGCTCC CTCTGAGTGG 600
GCTCGAAGAT TCCCAGGGAC TTACGCGTGC TGGAGAAGCA GAAGGCGGTG TTTGCCACCT 660
GACTCGTGGC TCCCGGGTCC TGGGCAAGGC TGCACCAAGG AGGGTCTAAA GATGATGCTT 720
CCCCTTTCTT GGCGTGGCCT CCGAAGGTCT CACAGGCCCC AACGGTCTCT CCGGATCTGG 780
GACTGCTGAT CTCCCTGGGA CAACTGCCAA CAGAGTGTCG TAGGCGCGGC CCTGGCAGGC 840
AGGGAGGCGC GTCCCTCACC GCTGGCCCAG AGGTTGCACT CAGTGCCCTG TCGCCGGACT 900
AGGACGAGGA TGTGGCCGCT GCACTTGCTC CCGCGGTGAC GTCACCGCCT CCTTCCGCTC 960
TGCGGCCTGG CGGTCTCCAT GGCAACCGCT GAAGCATCCA TCTCCTCTGC CATTGGCCGA 1020
CTGGCCGCAT TGAAATCAAG AGTCTGAGGG GGTCATTCGG AGGTGAGGGG TCGGCCACCA 1080
GCCCTCAGAA GCGCCCGCGA TTCTCCTTTG AATAATAGCC GATTCCAGGG GTGAGGGGAC 1140
AGCGAATGTA CAAGAGGCAC CCGGGGCATC 1170