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

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EnhancerAtlas ID
HS091-39855 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr5:179278950-179280370 
Target genes
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXP1MA0481.2chr5:179279338-179279350AAGTAAACAGTA+6.18
Foxa2MA0047.2chr5:179279335-179279347CCTAAGTAAACA-7.22
Nr2f6(var.2)MA0728.1chr5:179279064-179279079GAGGTCAGGAGTTCA+6.22
ZNF263MA0528.1chr5:179279696-179279717GAAGGAGAGGAAAGATGAGAG+6.07
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5179279400179279800
Number: 1             
IDChromosomeStartEnd
GH05I179852chr5179279263179280597
Enhancer Sequence
TGAGTGACAG AGCGAGACTC CGTCTAAAAA AAAATAAAAA AATAAAAAAT ATCAGGTGAA 60
GGCACTCACC AACATTATGA AATGTTTTTG TCTACGGAGG CAGGTGGATC ATTTGAGGTC 120
AGGAGTTCAA GACCAGCCTG GCCAACATGG TGAAACCCCG TCTCTATTAA ACATACAAAA 180
AACAAATTAG CTGGGTGTGG TGGCATGCAT CTGTAGTCCC AGATACTCAG GAGGCTGAGG 240
CAGGAAAACT GCTTAAACCC GGGAGGCGAA GGTTGCAGTG AGCCGAGATT GCGCCACTGC 300
ACTCCAGCCT GCATGACAGA GAGAGACTCC ATGTCAAAAA AAAAAAAAAC CCCAAAAAAC 360
AGCAATTTAA CTTTTAGGAC TTTGTCCTAA GTAAACAGTA AACAGCTGGT CACGTGGATA 420
AAGAGGTTTT TGTGAAAAGC TTCACGGTAG AGTTGTGCAT AACAGTCAAA AGGGAAATCA 480
ACCTAAATGC CCAACAAGGT TGGGCCAGTT CCTTACTCAC TCCACAAACA CCGAGCACTG 540
TGCTAGGTGC TGCGGATACA CCAGCAAATA AAAAGCCTCT GTTCTCACGG AACTTACAGC 600
CTTAGATGGA CAATCCGTGC ATAAACACAT GACTATGTAA CTTCCATAGG ATACTGAGAA 660
GAGGGAGGGG AACTCCACAG TGAGCACAAA GGCCTGAAGA GGGAGCAAAT TTGGGTTTAA 720
GGTCAGAAAG AAAGCACATG GCTGTAGAAG GAGAGGAAAG ATGAGAGGTG AAGGGAGAGG 780
TGGCACTGGG GCTGGAGCAG GAAAAGAGCA AGTTCAGTAA GGCAAAGGAT GCAGGACAGT 840
TTGGGGTCCT AGAGTTCAGG AGGGGCAATA CGGATGGACT GAAAAGACGT ACTGAATGCC 900
AGCTGCAAAC AGCTGGATGA GAGCATTTAC AGCCTGCCCC TGCCTGCCTC CACTTCCTGA 960
GCCCACTATC CCACACCTCC ACCTCCACCA ACGGCCTCTG CCCTTCCCCG GCTGCCCTGA 1020
TTCCTCTGTC ATCTTCTCAC AGTCCCCAGT GCTTTCCTTT CCTTGTGCTC AGCCGAGTTT 1080
TAAATTATGC AGATGCATGT GTGCATTAGT TTCTCTTCCC CTTCCACACA AGTGCATCTG 1140
TGAGGGCAAG AATGACAATG GGCTTACTTT CCACTGTTCC CCTTGTGCTT GGCACACAGA 1200
AAGTACTCAA GAAATACTTG CTGAATGAAG AATCAAATGG CAGTACCTTT CCAGATTCTG 1260
CTCCATCCAT TTCACTTCCT GAAGGAACAG GAAGCTCGGA AGCAGGAGCT CCGTGTCTGG 1320
GGAACTCTGT TTGAGAGAGG ATGATCCCAG CTGTGGCATG CTGGGACTCC CTGGAAGGGC 1380
TCGCTGCAGG CCTGCGCCCC ACTTGCTTTC TGTTTTGTAG 1420