EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-38915 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr19:10694750-10696110 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs148285494chr1910695350hg19
TF binding sites/motifs
Number: 35             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:10695330-10695348GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:10695334-10695352GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:10695338-10695356GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:10695314-10695332GGAGGGAGGGTAGGAGGG+6.07
EWSR1-FLI1MA0149.1chr19:10695302-10695320GGAGGAAGGGAAGGAGGG+6.33
EWSR1-FLI1MA0149.1chr19:10695914-10695932AGAAAGAAGGAAAGAAGG+6.55
EWSR1-FLI1MA0149.1chr19:10695318-10695336GGAGGGTAGGAGGGAAGG+6.56
EWSR1-FLI1MA0149.1chr19:10695289-10695307GTAAAGAAGGAAGGGAGG+6.6
EWSR1-FLI1MA0149.1chr19:10695285-10695303GAAAGTAAAGAAGGAAGG+6.86
EWSR1-FLI1MA0149.1chr19:10695918-10695936AGAAGGAAAGAAGGAAAG+6.95
EWSR1-FLI1MA0149.1chr19:10695926-10695944AGAAGGAAAGAAGGAAAG+6.95
EWSR1-FLI1MA0149.1chr19:10695310-10695328GGAAGGAGGGAGGGTAGG+7.13
EWSR1-FLI1MA0149.1chr19:10695930-10695948GGAAAGAAGGAAAGAAAG+7.22
EWSR1-FLI1MA0149.1chr19:10695297-10695315GGAAGGGAGGAAGGGAAG+7.41
EWSR1-FLI1MA0149.1chr19:10695350-10695368GGAAGGTAGGCAGGCAGG+7.45
EWSR1-FLI1MA0149.1chr19:10695922-10695940GGAAAGAAGGAAAGAAGG+7.85
EWSR1-FLI1MA0149.1chr19:10695293-10695311AGAAGGAAGGGAGGAAGG+8.05
EWSR1-FLI1MA0149.1chr19:10695322-10695340GGTAGGAGGGAAGGAAGG+8.16
EWSR1-FLI1MA0149.1chr19:10695346-10695364GGAAGGAAGGTAGGCAGG+8.29
EWSR1-FLI1MA0149.1chr19:10695326-10695344GGAGGGAAGGAAGGAAGG+9.47
EWSR1-FLI1MA0149.1chr19:10695342-10695360GGAAGGAAGGAAGGTAGG+9.79
IRF1MA0050.2chr19:10695951-10695972GAAGAAAAAAAGAAAGAAAGA-6
Nr2f6(var.2)MA0728.1chr19:10695038-10695053GAGGTCAAGAGATCG+6
SOX10MA0442.2chr19:10695612-10695623AAAACAAAGAA+6.62
ZNF263MA0528.1chr19:10695291-10695312AAAGAAGGAAGGGAGGAAGGG+6.02
ZNF263MA0528.1chr19:10695327-10695348GAGGGAAGGAAGGAAGGAAGG+6.24
ZNF263MA0528.1chr19:10695315-10695336GAGGGAGGGTAGGAGGGAAGG+6.36
ZNF263MA0528.1chr19:10695294-10695315GAAGGAAGGGAGGAAGGGAAG+6.47
ZNF263MA0528.1chr19:10695331-10695352GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr19:10695335-10695356GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr19:10695303-10695324GAGGAAGGGAAGGAGGGAGGG+6
ZNF263MA0528.1chr19:10695299-10695320AAGGGAGGAAGGGAAGGAGGG+7.57
ZNF263MA0528.1chr19:10695311-10695332GAAGGAGGGAGGGTAGGAGGG+7.82
ZNF263MA0528.1chr19:10695302-10695323GGAGGAAGGGAAGGAGGGAGG+7.89
ZfxMA0146.2chr19:10695016-10695030GAGGCCGAGGCGGG-6.01
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191069539110695723
Enhancer Sequence
GGGTGGAAGG AAAGGACCTG GTCACCACCA GCATCCAAGA ACCTACCACG CTGAGGAGGC 60
ACAGTGCCCG GTTCTGACCC TACTTCCTAG CTGAGGGGCT TGGGCAAGGC TCTGCCTCCT 120
TGTGCCTGTT TCCTGCTCTG TAAAATGGGA GTGTGATGAC AACAGCTAAT GGGTCTAGGG 180
CCCTCACTAA GTGCCAGGCT GTGTTTTATT AAAGGGTAGG CGATGGCTGG ACGCAGTGGC 240
TCACGCCTGT GATCCCAGCA TTTTGGGAGG CCGAGGCGGG TGGATCATGA GGTCAAGAGA 300
TCGAGACCAT CCTGGCCAAC ATGGTGAAAC CCCGTCTTTA CTAAAAATAC AAAAAATTAG 360
CCGGGCGTGA TGGCGTGTAT CTATAGTCCC AGCTACTCGG GGTGCTGAGG CAGGAGGATC 420
ACTTGAACCT GGGAGGCGGA GATTGCAGTG AGCCGAGATC GTGCCACTGC ACTCCAGCCT 480
GGCGACAGAG CAAGACTCCA TCTCAAAAGA AGAAAGAGAG AAAGAAAGAA AGAAAGAAAG 540
TAAAGAAGGA AGGGAGGAAG GGAAGGAGGG AGGGTAGGAG GGAAGGAAGG AAGGAAGGAA 600
GGAAGGTAGG CAGGCAGGCT GGCTACTAAA AAAAGAGTAG ATGTTTACTA ACTTATTAGT 660
TCTTGCCACA ACCCTGTGGG GTAGATGTTA TCATCATCTC CATTTCACAC AGGAGAAGTG 720
AGGTTAGAAA CCATGTCCAC TGGAAGCATA TGGAAACTGG GGATTGATCT AAGGCATCCT 780
GGGTCCAGAA TCCCTGCTGT TGCCCCAGAC TTCATTTGCA CCAAAGTGGG ATTATTTAAA 840
AAAACAACAA CAACAAAAAA AAAAAACAAA GAAGAGGCCA GGTGCAATGA CTCACTCATG 900
AAGACCAAGG CAGGAGGATC CCTTGAGGCC AGGAGTTTGA GACCAGCTTT GGCAACATAG 960
CGGGATCCCT CTACAAAAAA TTTCAAGAAT TAGCTGAGCA TGGTGGCCTG CACCTCTGTA 1020
GTCACAGCTA CTCTGGAGGC TAAGGCAGAA GAATCAATTG AGCCTAGGAG GTCGAGACTA 1080
CAGTGAGCTG TGGTCATACT ACTGCACTCC AGCCCGAGCA ACAGAGTGAG ACCCTGTCAA 1140
AAAAAGAAAG AAGAAAAGAA AGAAAGAAAG AAGGAAAGAA GGAAAGAAGG AAAGAAAGAA 1200
AGAAGAAAAA AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA 1260
GAAAGAAAGA AAGAAAGAAA GATGACAGTT CATATGATTG TGCCTGGTAG TCAGGAAGAC 1320
ACCCATAATA GTAAACACTT CTGTCTGGAC ACGGTGGCTC 1360