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

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EnhancerAtlas ID
HS175-23995 
Organism
Homo sapiens 
Tissue/cell
SK-N-MC 
Coordinate
chr5:74832190-74833620 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RFX1MA0509.2chr5:74832318-74832334TGTTTCCATGGCAACA-6.89
RFX1MA0509.2chr5:74832318-74832334TGTTTCCATGGCAACA+6.91
RFX2MA0600.2chr5:74832318-74832334TGTTTCCATGGCAACA+7.11
RFX2MA0600.2chr5:74832318-74832334TGTTTCCATGGCAACA-7.17
RFX5MA0510.2chr5:74832318-74832334TGTTTCCATGGCAACA+7.05
RFX5MA0510.2chr5:74832318-74832334TGTTTCCATGGCAACA-7.06
RREB1MA0073.1chr5:74832417-74832437GTGGTGGGGGTGGGTGGAGG-6.32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr57483282274832998
Enhancer Sequence
AACATGAGGT TGTGCCTGCC TGCAGAGTTC AGGTGGAAGT GGGAACCCTG GATTGGAAGT 60
TCTCGTAGAT GTGGCCCATC TGGCTACAAG AGGCAGGGTG GGTTGAATTG CCTGCTCTGC 120
CATCTGGGTG TTTCCATGGC AACAGGAGGC TGTACCCCCG GCAAATTCAG GCAGAAGCAG 180
GACCACTGGG CCAGAAGCTC TAGCAGGCAT GGCTCACCTG GCTACCAGTG GTGGGGGTGG 240
GTGGAGGCAC CCACCCTGCC CCCTGGGTGT TTGCTGGGAC AATAGTAGGC TGTGCCTACC 300
AGCTGAGTTG CCATAGAAGC AGGACCCCTG GGCCGGAAGC TCTAGCATGT GTTGCCCCCC 360
AGCTACCAGA GGCAGGGATG GGCAGGGTGA CATGCTGTCT TGTCTGGGTG TTTACTGGGA 420
CAACAGGAAG CTGAGCCCTC CTGCTGAGTT CACACAGATG TGGAGCTGCT GGGCTGGAAG 480
CTCTCACAAG CATTGCTTGC CTGGCTACCA GTGACGGGGG CGGGTAGGGT CATGTAGTTT 540
GCTGTCCCAG CATTTCTTGG GATGACAGAA AGCTGCATCC TTCAGCTGAG TTCACACAGA 600
AGCAGGACTG CTGGGCTAGA AGCTCTAGCA AGCATTGTCT GCCTGGCTAC CTGTGGCAAG 660
GGTAGATGGA GTGGCCAGCC AAATTCTGGC TGAAGCAGGA CCACTGGGCT GGAGGCTGTT 720
GCTGAGCCCC ATCCAGCAAG GAGTAGTGGA GAAATCTTAC TGCTTTCAGG CACTGCAGTG 780
GCGGCCTCTA TTGAGGCTAT AACACTGGTG CTGATCTGCT CCGGGGCGCA AAGCTTGTAG 840
AGGTGCCCTT GGGCTTCAGA ATTGCCTCCA CCAAACATCT CAGTGGCTCT GCCTCAGTCT 900
AGAAGCATGG GGGTGGGGGG CACAGGGTGG TCAGGGGGAA TCTCCCATTC CCAGTCTTGC 960
ACAGGTTTCT GTGGAAAGTG TGAATCCCCC TGGGGGCTCT CACTCACCGT TTGCGGTGTT 1020
GGTTAGGTTC TCCTGGCTCT GTGCTCAGCC CAGACAAGCT GGTGCCCACC TTCATTCCTC 1080
CGTGCTCTCT GTGTTTCCCT GCTGCCTTGA TAGATCTCAA CGTTGTTTCT CAGATGATCA 1140
GCTTGCAGGG TCAGTGTTCA GTAGCCCTTT TGCTTATTCT CTGTGAGAGC AATGCGCATG 1200
AGCTGCTTCT AGTCTGCCAT CTTGGCCCCC CTAACCTAAC CCATTTTTAG ATGTTACATT 1260
CCATCACTTC TACTTCTGCT ATAATCTATT TGTTAGAAGC AGGTCACTTA ATTACACATT 1320
ATGGCATTAG TTTGTTGTGC CTTTTGTGCT TTTCCTAGCA TCTGTGAAGT ATTATTGAAA 1380
GTATTTTAGT AGTGTTAGGA AATGTGTATT TTATAATAAT TATTTTAGTA 1430