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

TagContent
EnhancerAtlas ID
HS111-02735 
Organism
Homo sapiens 
Tissue/cell
KB 
Coordinate
chr19:47759870-47761580 
Target genes
Number: 3             
NameEnsembl ID
TF binding sites/motifs
Number: 26             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr19:47761553-47761568TGGCCTTTGTCCTTT-6.46
KLF14MA0740.1chr19:47760482-47760496CAGGGGGCGTGTCC-6.09
KLF16MA0741.1chr19:47760273-47760284GGGGGCGGGGC-6.02
KLF16MA0741.1chr19:47760305-47760316GGGGGCGGGGC-6.02
KLF16MA0741.1chr19:47760550-47760561GGGGGCGGGGC-6.02
KLF16MA0741.1chr19:47760678-47760689GGGGGCGGGGC-6.02
KLF16MA0741.1chr19:47760484-47760495GGGGGCGTGTC-6.32
KLF4MA0039.3chr19:47761255-47761266ACAGGGTGTGG-6.14
KLF5MA0599.1chr19:47760049-47760059GGGGCGGGGC-6.02
KLF5MA0599.1chr19:47760274-47760284GGGGCGGGGC-6.02
KLF5MA0599.1chr19:47760306-47760316GGGGCGGGGC-6.02
KLF5MA0599.1chr19:47760551-47760561GGGGCGGGGC-6.02
KLF5MA0599.1chr19:47760679-47760689GGGGCGGGGC-6.02
SP1MA0079.4chr19:47760735-47760750CGTGGGCGGGGCCAG-6.01
SP1MA0079.4chr19:47760114-47760129TGTGGGCGGGGCCAT-6.28
SP1MA0079.4chr19:47760677-47760692TGGGGGCGGGGCCAG-6.43
SP1MA0079.4chr19:47760180-47760195TGTGGGCGGGGCCAG-6.44
SP1MA0079.4chr19:47760304-47760319AGGGGGCGGGGCCAG-6.57
SP4MA0685.1chr19:47760270-47760287GGCGGGGGCGGGGCCAC-6.03
SP4MA0685.1chr19:47760481-47760498TCAGGGGGCGTGTCCAG-6.03
SP4MA0685.1chr19:47760112-47760129ACTGTGGGCGGGGCCAT-6.05
SP4MA0685.1chr19:47760178-47760195TCTGTGGGCGGGGCCAG-6.17
SP4MA0685.1chr19:47760302-47760319CCAGGGGGCGGGGCCAG-6.42
SP4MA0685.1chr19:47760675-47760692GGTGGGGGCGGGGCCAG-6.78
SP8MA0747.1chr19:47760483-47760495AGGGGGCGTGTC-6.27
ZfxMA0146.2chr19:47759941-47759955CAGGCCCGGGCGGG-6.23
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_47872chr19:47760557-47761945Pancreas
SE_65460chr19:47758823-47764848Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194776020047760600
Enhancer Sequence
CCTGGGGGAG GGGGCCGGGA GCGCGCCCAG AGAAGGCGGG GCCTGAAGCC CCACGTGGCG 60
GGGAGTGCGA ACAGGCCCGG GCGGGGTCGG AGTTCTCTGC GGGGGGCGGG GACAGGACGC 120
CCACATGGGA AGCTGGAGGG GCGCTGGCGG GGCGGGCCGT TGGGTGGGTG GGCAGGGTCG 180
GGGCGGGGCG TGGCCAGAGC CTGGGCCGGC GGCTGTGGGC GGGACCTAAA AGTTGTGGCT 240
GGACTGTGGG CGGGGCCATA GTGTTGCTTG TTCAGCTGTG TGGCGGGGCT CGGACGCCGG 300
GCGGAAGCTC TGTGGGCGGG GCCAGAAAGT TTTGCCTTAC TGGAAGTGGG TCCAGATTCT 360
TGGCCGGGAC GTTGGGGGCG GACCCAGAGG CTGACGCAAT GGCGGGGGCG GGGCCACAAT 420
GTAGTGGGGG AGCCAGGGGG CGGGGCCAGG GTGCTGGCGG GGAATGCTGG GGGTGGAGCC 480
AGAAAGTTTC GTCTGAGCCA CGGGCGCGGC CAGAGCGTTG GCCGGGAGGC GGGGAAGCGG 540
GGAGTTGAGC CAGAACCCTG GGGAAGCCAT GGGCGGGGCC AGATGCTGAC GCAACGAGGT 600
GTGGGAGGGA GTCAGGGGGC GTGTCCAGGA GGTTGGCCAG GCCAATCGGA GGCGGGGCCA 660
GAGGGTTGAC TGGGCAGGCC GGGGGCGGGG CTGGAATAAT AATAAGAGAT GGTAGGGGCG 720
GGTGTAGGCT GTTGCCTGCG AGCCAGGAGG CGGGGAAAGA GCGTGGCTGG GAAAGTCGGG 780
AGCGGGGCCA CATTAATGGC CCATGGGTGG GGGCGGGGCC AGAAGTCTGG CGGGAAAGGC 840
GGGGCCAGAA AGTTTTTTCC CGAGCCGTGG GCGGGGCCAG AGCGGTTTCC AGGATGTCGG 900
GGACGTGGCC CTGGCATTCC CAGCCGGATT GAGGCTGGAG CTTTGCACAG AAAATCTGGG 960
GCGGGCCTGG GTAGTTTTGT CCTTGTTGGG GCGGGTGGAG TATTCAGTGG GGCAAAACGC 1020
CAGTTCCAGG AAGCCTCGCC AGTGAGTTCT GGGCCTGTGT ACAGAATCCT TTCGGGGGAG 1080
GCGGGAGGCT GTCGACCTTC CGTAGGGCGC TGGAGACGGG ACTAGGACGT CCCTGAGGAA 1140
GGCGCGGGCT TGGAATGTTC TCTGAGAGCT TGGGCAGCCA ATAAGAGTGG GGTTCGGACT 1200
TTCTTTGAGC GTGGGATTGG GAATGTTTCT GAACCTTACC TGGTGGAGCT AGAATATTCG 1260
CCTGGATATG AGAGGCACCA GGATGAGCAC AGGGAGGTGG GTCTGGAACT TTCTTTTGCA 1320
GGCTGGTTGG AGGGGTTGTA GTTGGAACTC TCTTGAGATA GGGAACCCGG GCTAACACTC 1380
ATACCACAGG GTGTGGCGGC TGGCCTAGAA TCAGCCTTTG GAGGAGAGCA GTGTTGGATA 1440
CTTAAGCAGT GGGTGGGGGC CAGAACATCC CCAAGGTGGG TTTGACTAGA TCGTTTACAT 1500
GGGAACTGGG TGAGTCCACA AAGATCATGA AAGGGCTGAG TCTGAATTTC TATGGAGAAG 1560
ATGGAGGTGG CAGTTGAAAG GAGGGAGAGT GAGGGCTACA ATTCTCTTGG GGTACAGGGT 1620
TTTTTGTGTA TGGCTGTGAG GATCCCGCAG TATGTTAGAG GGTGAAGTAG GTTGGGGGGC 1680
CATTGGCCTT TGTCCTTTTT TTCCCTCTGT 1710