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

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EnhancerAtlas ID
HS139-22498 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr17:18020440-18021890 
TF binding sites/motifs
Number: 12             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr17:18021565-18021580AGGGTTCAAAGTTCT+6.02
RESTMA0138.2chr17:18020742-18020763GGCAGAACCAGGGCCAGAACC+6.22
RFX1MA0509.2chr17:18021786-18021802TGTTGCCATGACGACT+6.14
RFX1MA0509.2chr17:18021786-18021802TGTTGCCATGACGACT-6.15
RFX2MA0600.2chr17:18021786-18021802TGTTGCCATGACGACT+6.07
RREB1MA0073.1chr17:18021376-18021396CCCCAACACACACACACACA+7.29
ZNF263MA0528.1chr17:18020531-18020552TGGGGAGGAGGAGCAGGAAGA+7.22
ZNF263MA0528.1chr17:18020540-18020561GGAGCAGGAAGAAGAGGAAAG+7.82
ZNF263MA0528.1chr17:18020537-18020558GGAGGAGCAGGAAGAAGAGGA+8.39
ZNF263MA0528.1chr17:18020534-18020555GGAGGAGGAGCAGGAAGAAGA+8.48
ZNF263MA0528.1chr17:18020865-18020886GGAGGAAGAGGAGGAGGAGAG+8.94
ZNF263MA0528.1chr17:18020862-18020883TGAGGAGGAAGAGGAGGAGGA+9.51
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr171802107718021400
chr171802060018020978
Enhancer Sequence
CCATCCCTGT GAGACTGCCT GCACCAGGCA CCAACAGCCC CTGGTGCAAC TCCTCTGAGT 60
GGCTGGGCAC TGACTGGCTC CAGGTGAATC TTGGGGAGGA GGAGCAGGAA GAAGAGGAAA 120
GTGAAGAGCC AGAGAAAGTG AGCAGGGGGA AGAGGCAGAC AGAGAGGGGG AGACCTCACT 180
TGCTGCATGG TCCCCTCTCT GCTCCTGCCA CTTACCTGGG AAGGCCTCAC CCTGTCCCTG 240
TTTCACAGCT GAGCACGTTG AGGCTCTGAA GCCACTGATC TGAGGGCGTG GAGCTGGCAA 300
GTGGCAGAAC CAGGGCCAGA ACCTTGCTGC TTTGGGGTCT CCTATGCTAA ACCTTAAACA 360
ACCAAAGAAT TAGCTCTGGG ACCAAAAGAG TGAACCAGAG TTCAGTGAGT TGAGGTCCAT 420
CTTGAGGAGG AAGAGGAGGA GGAGAGCTGG TTCTGAGGCT TCAGGTCTCA GAGCTGCCAC 480
TCCCCACCTC CGCTGGCCTG CCCAGTTTTT CCCACCCCCT ACCTCTTTTA GTGCAGGTTC 540
TCAAAAGTGA GTTAGACTGG CCACCAACCA GACTTTGGAC ATGCAGCCTT AGGTCAGGCC 600
ATATGAAGCA ATCAGCTATG CCCAGAGAAG GCAGTAACCA CATGGCCACA GCCTACTCAG 660
CCAGGGCAGA AAGTAAGAGG AGAGGACAGG GCTAGGCAGG GACCCCAGAA AGGAGCCAGC 720
AGGAGGCATC TCCAGTTACC CAGCAGCTCC ATCAGGTCTT GCTTCCTTTT GGTGAAGGAG 780
ATGGGGCATA GCTTATCACT CCCATTCTTC AGAGGAAACT GAGGCCCAGA GAGGACAAGG 840
ACTTTCCTGG ACCCACACAG CCAGTCAGTG ACAGAGCCTA GGGTCTGAGC CAGGCCTGAC 900
CCAACCTCCA TTTCTGCCTC TCTACCCCTG CCCCCGCCCC AACACACACA CACACACAAG 960
TGGAGTTCCA CTGAAACGCC CCTCCTTGCC CTGCCTTCTG AGCCGGCAGC CTGGCTCCCC 1020
ACCCCATGTA TTATTCAGCT CCTGAGAGCC AGCCAGCTCC TGTTACACTG ACCGCAGCCC 1080
AGCACCTGCT CTGCCCATTC CCCTCCTCCC TTGCCTAGGA CCTAGAGGGT TCAAAGTTCT 1140
CCTCCAAGAT GACTTGGTGG GCTTTGGCCA TCCCACCCTA GGCCCCACTT CTGGCCCAGT 1200
GCAGGTGTGC TGGTGATTTA GGGCAGGTGG CATTCCATCT CTGTGGCTCA ATGTCTTCCT 1260
CTGTGAAGCC GAAGTGACCC AAGGGCTCCC TTCATGGGGT TGAGCCAGCT GTGGCCCAGG 1320
GAGGGCCTAA CCAGGATGAG CACTGATGTT GCCATGACGA CTCCGAGGCC AGAATGTCTC 1380
CCCCAGCACA GGCCTCATAG GCAGGCTTCC CCATCCTGGT AAACAACACC CACACACTTT 1440
CTACTACTGC 1450