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

TagContent
EnhancerAtlas ID
HS091-00023 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr1:1000610-1001780 
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BHLHE40MA0464.2chr1:1001171-1001181GTCACGTGAT-6.02
HNF1AMA0046.2chr1:1001711-1001726AGCTAATGATTAATA-6.08
HNF1BMA0153.2chr1:1001712-1001725GCTAATGATTAAT+6.22
MITFMA0620.2chr1:1001167-1001185GCAAGTCACGTGATCACA+6.31
MITFMA0620.2chr1:1001167-1001185GCAAGTCACGTGATCACA-6.31
PLAG1MA0163.1chr1:1000664-1000678GGGGCCCTGGGGGG+7.03
RREB1MA0073.1chr1:1000639-1000659CCTCGGGGGGTGTGGTGGGG-6.41
RREB1MA0073.1chr1:1000669-1000689CCTGGGGGGGTGTGGTGGGG-7.16
TCF3MA0522.2chr1:1000949-1000959AGCAGGTGTT-6.02
TFEBMA0692.1chr1:1001171-1001181GTCACGTGAT-6.02
USF2MA0526.2chr1:1001167-1001183GCAAGTCACGTGATCA+6.05
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr110008311000953
chr110007361001492
Number: 1             
IDChromosomeStartEnd
GH01I001061chr19969711001049
Enhancer Sequence
CTGGGGGGGT GTGGTGGGGT CTGCGGTGCC CTCGGGGGGT GTGGTGGGGT CTGCGGGGCC 60
CTGGGGGGGT GTGGTGGGGT CTGGGGGGCC CTAAGCTTAG ATGCAGGTCT CTCCCTGGCA 120
GCCCCTCAAG GCCACGAGGA TCAGTGCTCG GAGCCTGGAG GGCTGTGTGC AGGAGTAGCA 180
GGGCCACTGA TGCCAGCGGG AAGGCCAGGC AGGGCTTCTG GGTGGAGTTC AAGGTGCATC 240
CTGACCGCTG TCACCTTCAG ACTCTGTCCC CTGGGGCTGG GGCAAGTGCC CGATGGGAGC 300
GCAGGGTCTG GGACTGTAGG GTCCAGCCCT ACGGAGCTTA GCAGGTGTTC TCCCCGTGTG 360
TGGAGATGAG AGATTGTAAT AAATAAAGAC ACAAGACAAA GAGATAAAGA GAAAACAGCT 420
GGGCCCCGGG GACCACTACC ACAAAGACAC GGAGACCGGT AGTGGCCCTG AACGGCTGGG 480
CTCGCTGATA TTTATTGCAT ACAAGACAAG GGGGCAGGAT AAGGAGGGTC AGTCTTCTAA 540
GTGATTGACA AGGTGAAGCA AGTCACGTGA TCACAGGACA GCGGGCCCTT CCCTCTTAGG 600
TAGCTGAAGC AGAGAGAGAA GGCGGCAGGC ATCAGCGTTT TCTTCTATGA ACTTATAAGA 660
TCAAAGACTT TAAGACTTTC ACTATTTCTT CTACCGCTAT CTACTACGAA CTTCAAAGAG 720
GAACCAGGAG TACGGAAGGA GCATGAAAGT GGACAAGGAA CGTGACCATT GAAGCACCAC 780
AGGGAGGGGT TCAGGCCTCC GGATGACTGC AGGCAGGCCT GGGTAACATC CAGCCTCCCA 840
CAAGAAGCTG GTGGAGCAGA GCGTTCCCTG ACTCCTCCAA GGAAAGGAGA CTCCCTTTCC 900
CGGTCTGCTC AGTAACGGGT GCCTTCCCAG ACACTGGCGT TACCGCTTGA CCAAGGGGCC 960
CTCAAGCGGC CCTTATGCGG GCATGACAGA AGGCTCCCCT CTTGCCTTCT ATTCACTTCT 1020
CACAATGTCC CTTCAGCACC TGACCCTATA CCTGCCGGTT ATTCCTAGGT TATATTATTA 1080
ATGCAACAGA GTAATATTAA AAGCTAATGA TTAATAATGT TTATAATAAT GATGGATAAT 1140
TGTTCATGAT CATCGCTGTA TCTAATTTGT 1170