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

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EnhancerAtlas ID
HS108-07218 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr11:34182770-34184120 
Target genes
Number: 2             
NameEnsembl ID
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nkx2-5(var.2)MA0503.1chr11:34183077-34183088AGGCACTCAAG+6.14
TFAP2CMA0524.2chr11:34183997-34184009TGCCCTGGGGCT-6.11
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr113418327834183763
Number: 1             
IDChromosomeStartEnd
GH11I034160chr113418254434185939
Enhancer Sequence
TTCCTGGGCA TGGAGTGGCC CTCTCAGGAT GGCCATAGAA TGAAAGCTTT AATTCATTCT 60
AATAGGTCTT GCTGGCAGGT CAGAGTGGAG TTTCAGGTTC TCATGAGATG AGGTGGAGGA 120
ATGGCTTCGG CCCAAATGCA GGGAACTCAA GCTCTGAAAG TTGACCGCCC AGCCTGGGGA 180
TTTGGAAGTA TGGGCCCAGC ACCCAAAGTA GCCTTGTTGC TTAGTGGGCT CAAGAATTAC 240
TTGCTAGAGA GGTCTCATTA GTTGTGGAGG GGTGGCCAGG AGGGCTTGGA TGGCCAGAGA 300
ATATGCCAGG CACTCAAGGA CACACAGGCC TCCTTGTCTG CACGGAAGCT TGAAACGAAC 360
CCGGTCCTAT CACGAGGGGC TCTCCAGCAC ACAGAGCACT GGAAAGCCGC TGCACATCCC 420
CAGGCACATA ATGACTGTTT TACAGTTCCC CAGCATGTGT CAGTGGGGCT GTAACTTAAC 480
ATTGCTGTGG GAAGTTCATG ACATAAACTA GTCCTGTCCC TGGTAATTAG AGAGACAGCT 540
TCTTACCCCA ACCTCACTGT GGATCAAAGA ACTGACGGCA TTCCCCAGCG ACACATTGAC 600
AGTAGTGTGG TGTGTTAGTA TCCTTGGGTT ATTGACTGCA GGTGGGAGTG ACGTCTCTGT 660
TTTACGGTGA AGAACACTGA GGCTGACTCA CTGCTGTCTT GGCCCGGCCC TGGGGGTTTG 720
TGGCCTTGTG ATGACAGTGA CGGTGCTGTC ATCCACCAAG TGCTCACGGT GGCCACTACG 780
CCTTGTACTT CAGGTGATGT CACCTCATTC TTAGATAAGG ATCATTAGCA CCAAAGCCAC 840
AGAGGTGGGA GTTGAGGCTT GGAGAGAGGA CGTGGTATGC AGCTAACACA GGACCTGACC 900
TAAGTCTGTC TGACTAGCCT CCCTGGAGGA CACCAAAAGT CCACAGACTC GCAGACCCAA 960
GGAGTGCAAG GTCAGCCGAG TGACAGGACT GCCGCCTCAC AGCGTGGAGT CCCGGGGCTT 1020
CAGAGGCTCC CAGTGCTCGA CATCCCTGGG CTGTGACTGG GGAGGGGGCA GCGAAGCTCC 1080
AGCCAGGCAG GGTGGAGGGC CCGAGGGCAG GGGACTGGGC CATGACCCCA AGACGTGGCA 1140
CTGTTGAGCA CTGTCTGAGG CCCAGGGCCC CTCCTGAACT GGCCGTGTAG CAGGGGGGTC 1200
CCAGCCTCCA CCCAGTCTGT GCTCAGCTGC CCTGGGGCTT GTCTGTCCCT GCAGGCCCTG 1260
GCCCTCTCAG GCCTGCTGAA GAGCAGCAGG GAGTGACCGT GTGTGTCCAT ATGCATGCAT 1320
GGACATGGGT GTGCATGCCC GTGAGGCCTC 1350