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

TagContent
EnhancerAtlas ID
HS091-24410 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr19:47798920-47799810 
Target genes
TF binding sites/motifs
Number: 27             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr19:47799557-47799576TCTCCACAAGGGGGCGCCA+7.2
EWSR1-FLI1MA0149.1chr19:47799734-47799752ATTTCCCTCCCTCCTTCC-6.4
EWSR1-FLI1MA0149.1chr19:47799786-47799804CCTCCCTCCCTTCCTTCT-6.71
EWSR1-FLI1MA0149.1chr19:47799770-47799788CCTCCCTTCCTCCCTCCC-6.88
EWSR1-FLI1MA0149.1chr19:47799766-47799784CCTCCCTCCCTTCCTCCC-6.92
EWSR1-FLI1MA0149.1chr19:47799762-47799780CCTCCCTCCCTCCCTTCC-7.08
EWSR1-FLI1MA0149.1chr19:47799782-47799800CCTCCCTCCCTCCCTTCC-7.08
EWSR1-FLI1MA0149.1chr19:47799754-47799772CCTTCCTCCCTCCCTCCC-7.28
EWSR1-FLI1MA0149.1chr19:47799774-47799792CCTTCCTCCCTCCCTCCC-7.28
EWSR1-FLI1MA0149.1chr19:47799738-47799756CCCTCCCTCCTTCCTTCC-7.97
EWSR1-FLI1MA0149.1chr19:47799750-47799768CCTTCCTTCCTCCCTCCC-8.32
EWSR1-FLI1MA0149.1chr19:47799746-47799764CCTTCCTTCCTTCCTCCC-9.47
EWSR1-FLI1MA0149.1chr19:47799742-47799760CCCTCCTTCCTTCCTTCC-9.72
ZNF263MA0528.1chr19:47799761-47799782CCCTCCCTCCCTCCCTTCCTC-6.54
ZNF263MA0528.1chr19:47799749-47799770TCCTTCCTTCCTCCCTCCCTC-6.86
ZNF263MA0528.1chr19:47799738-47799759CCCTCCCTCCTTCCTTCCTTC-6.96
ZNF263MA0528.1chr19:47799745-47799766TCCTTCCTTCCTTCCTCCCTC-7.08
ZNF263MA0528.1chr19:47799785-47799806CCCTCCCTCCCTTCCTTCTCT-7.11
ZNF263MA0528.1chr19:47799757-47799778TCCTCCCTCCCTCCCTCCCTT-7.14
ZNF263MA0528.1chr19:47799777-47799798TCCTCCCTCCCTCCCTCCCTT-7.14
ZNF263MA0528.1chr19:47799773-47799794CCCTTCCTCCCTCCCTCCCTC-7.19
ZNF263MA0528.1chr19:47799753-47799774TCCTTCCTCCCTCCCTCCCTC-7.29
ZNF263MA0528.1chr19:47799782-47799803CCTCCCTCCCTCCCTTCCTTC-7.38
ZNF263MA0528.1chr19:47799769-47799790CCCTCCCTTCCTCCCTCCCTC-7.5
ZNF263MA0528.1chr19:47799742-47799763CCCTCCTTCCTTCCTTCCTCC-7.75
ZNF263MA0528.1chr19:47799762-47799783CCTCCCTCCCTCCCTTCCTCC-7.9
ZNF263MA0528.1chr19:47799765-47799786CCCTCCCTCCCTTCCTCCCTC-8.23
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194779927247799758
Number: 2             
IDChromosomeStartEnd
GH19I047295chr194779924147799390
GH19I047296chr194779948147799670
Enhancer Sequence
TTCTAGACCA CCCTGGGCAA CATGGCAAAA CCCTGTCTCT ACTAAAAATA CAAAAATTAG 60
CCAGGCATGG TGGCACACGC CTGTAAACCC AGCTACTCGG GAGGCTGAGG CAGGAGAGTC 120
GTTTGAATCC GGGAGGTGGA GGCTGCAGTG AGCCGAGATT GCACCACTGC ACTCCAGCCT 180
GGGTGACAGA GCAAGACTCT GTCTAGAAAA AAAAAAAAAG AATACAAATT GCTTATTTCC 240
AAGAAAACAT CTCTGCCGTG CTTTCAGATT TTCAGCTGAT TACAAATCAC GCACCCATGA 300
TCAAATCCAA CAAGAGATAG ACCCCCTGCC ATAAAGGAAG AAGGCTGGCT GGGTGTAGTG 360
GCTTATGACT GCAATCCCAG TGCTTTGGGA GGCTGAGGCA GGAGGATCTC CGAGGCCAGC 420
AGTTCAAGAC CAGCTTGAGC AATATAGCGA GACACCCCCT CATCTCTCCA ATAATAATAA 480
AAAAAATCAG CCAGGCATGG TGGCGCGTGC CTGTAGTCCA ATCTACTCGG GAGGCTGAAG 540
TGGGAAGATT GCTCCAGGAG TTCGAGTCTG CAGTTGGCTG AGATCTCGCC ACTGCACTCC 600
AGCCAGGGCG GTAGAGCCAA ACCTTGTCTC AATAAAATCT CCACAAGGGG GCGCCATCTA 660
CATGATGATA GCAGGAAGGG AACCGGCCAG TGTCTCCTGG TGACGTACTC ATTCAGCGCT 720
TCTTATACCT TAAAGGTGAC CAGGAATCAC CTGGGGGTCT TGTTAAAATG CAGGTTCTAA 780
TTCAGCAGGG CTGGAGCAGG ACCACAGCTC TTGCATTTCC CTCCCTCCTT CCTTCCTTCC 840
TCCCTCCCTC CCTCCCTTCC TCCCTCCCTC CCTCCCTTCC TTCTCTTTCT 890