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

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EnhancerAtlas ID
HS176-19219 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr19:47792320-47793580 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr19:47792806-47792817CATGAGTCACC-6.62
JUNDMA0491.1chr19:47792806-47792817CATGAGTCACC-6.02
POU2F2MA0507.1chr19:47792980-47792993ATATGCAAATCAA-6.87
Pou2f3MA0627.1chr19:47792978-47792994TTATATGCAAATCAAG+6.31
RFX1MA0509.2chr19:47793081-47793097TGTTGCCATGGCAATG+6.14
RFX1MA0509.2chr19:47793081-47793097TGTTGCCATGGCAATG-6.17
RFX2MA0600.2chr19:47793081-47793097TGTTGCCATGGCAATG-6.66
RFX2MA0600.2chr19:47793081-47793097TGTTGCCATGGCAATG+6.67
RFX5MA0510.2chr19:47793081-47793097TGTTGCCATGGCAATG+6.92
RFX5MA0510.2chr19:47793081-47793097TGTTGCCATGGCAATG-7
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194779245947793541
Number: 1             
IDChromosomeStartEnd
GH19I047288chr194779172147793777
Enhancer Sequence
ACTTTGAAAG GCTGAGGTGG GAGGGATAGC ATGAGGCCAG TAATTTGAAA CCAGCCTAGG 60
CAACATAGCA AGACCCTGTC TCTATAAGAG AAAAATTTTT AAAAATTAGG TGGGCTTGGT 120
GATGTGTGTC TACAGTCTCA GTATTGGGGC TTAGCCTGGG AGGGTTCTTG ACTTTGCCCA 180
TGTAAGAATT CAAGGGTGAG CCAGTGGTGT TATTTTTTTT TCTTTTTCCT TTTTTGAGAC 240
AGAGTGTTGC TCTGTCACCC AGGCTGGAGT GCAGTGGCAT GATCTCAGCT CACTGCAACC 300
TCCACTTCCC GGTTTCAAGT GATTCTTGTG CCTCAGCCTC CCAAGTAGCT GGGATTACAG 360
GCATGTGTCA CCGTGCCCGG CTAATGTTTT GTGGAGGTGA AGTTTCACCA TGTTGCTGGC 420
TGGTCTTGAA TTCCTGGCTT CAAGTGATCC ACCCACCTCG GGCTCCCAAG ATGCTGGGAT 480
TACATGCATG AGTCACCGTG TCTGGCTCAG TGGTGTTAAA TAGCAACTTT TACTGAAGCC 540
TCAGTGCACA GCTGCAGCAG AGGAATTGCC CCTTGCAGAG CGGGGCTACC CCACAGGCAG 600
TGTGCCCAGA AGAGCAGCCC AGAGGCAGCA CTGCTGTCAT ATTTATACCC ACTTTTAATT 660
ATATGCAAAT CAAGGGGCAG TTTATGCAAA AATTTCTAGG ATGAGGGTGG TAATTTCCAG 720
TCACCGGGTC ATTGCCATGG AAAGTGGTGC TAAGGTCCGA GTGTTGCCAT GGCAATGGTA 780
AACTGATACG GTACACTGGT GGGTGTGTCT TATGGAAAAC TGCTTTTGCC CTAGACCTGT 840
TTCAGCCAGT CCTCAGTTTG GTCCTGTGTA CAAGCCCTGC CTCCTACCTC AGTAGGGTAG 900
GGCACTGGGC AGAACTGTGT GACTCCCATT CCAGGCCCCA GCTCCTGGAG GACATTTCGA 960
ACACACCGTG AGGGGGAAGG GAAGCTGCTG TGTTGAAGGT AAGGACCCAG TCCTGGCAGG 1020
TTCATCACCT GCTGACTAAA GAGCCCTTGG GCCCTGAATA ATCAGCAGCG GTGGCCAGGC 1080
CAGGTGGTTC ACGCTGTGGG CCTTAGGTGA GACTCAAACG TGATGGCTTC AGGTGGAACC 1140
TGGCACATTC CCGGCTGTGG TGGCTACATG GGAGAGACTC CTTCTGCTTG AGAAAGCAGA 1200
GAGGCCAGGC GTGGTGGCTC ATGCCTGTAA TCCCAGCACT TTCTGATCAA GTGGATCACC 1260