EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS020-21631 
Organism
Homo sapiens 
Tissue/cell
CD34+ 
Coordinate
chr19:10695030-10696450 
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)MA0728.1chr19:10696156-10696171GAGGTCAAGAGTTCG+6.24
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
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191069539110695723
Enhancer Sequence
TGGATCATGA GGTCAAGAGA TCGAGACCAT CCTGGCCAAC ATGGTGAAAC CCCGTCTTTA 60
CTAAAAATAC AAAAAATTAG CCGGGCGTGA TGGCGTGTAT CTATAGTCCC AGCTACTCGG 120
GGTGCTGAGG CAGGAGGATC ACTTGAACCT GGGAGGCGGA GATTGCAGTG AGCCGAGATC 180
GTGCCACTGC ACTCCAGCCT GGCGACAGAG CAAGACTCCA TCTCAAAAGA AGAAAGAGAG 240
AAAGAAAGAA AGAAAGAAAG TAAAGAAGGA AGGGAGGAAG GGAAGGAGGG AGGGTAGGAG 300
GGAAGGAAGG AAGGAAGGAA GGAAGGTAGG CAGGCAGGCT GGCTACTAAA AAAAGAGTAG 360
ATGTTTACTA ACTTATTAGT TCTTGCCACA ACCCTGTGGG GTAGATGTTA TCATCATCTC 420
CATTTCACAC AGGAGAAGTG AGGTTAGAAA CCATGTCCAC TGGAAGCATA TGGAAACTGG 480
GGATTGATCT AAGGCATCCT GGGTCCAGAA TCCCTGCTGT TGCCCCAGAC TTCATTTGCA 540
CCAAAGTGGG ATTATTTAAA AAAACAACAA CAACAAAAAA AAAAAACAAA GAAGAGGCCA 600
GGTGCAATGA CTCACTCATG AAGACCAAGG CAGGAGGATC CCTTGAGGCC AGGAGTTTGA 660
GACCAGCTTT GGCAACATAG CGGGATCCCT CTACAAAAAA TTTCAAGAAT TAGCTGAGCA 720
TGGTGGCCTG CACCTCTGTA GTCACAGCTA CTCTGGAGGC TAAGGCAGAA GAATCAATTG 780
AGCCTAGGAG GTCGAGACTA CAGTGAGCTG TGGTCATACT ACTGCACTCC AGCCCGAGCA 840
ACAGAGTGAG ACCCTGTCAA AAAAAGAAAG AAGAAAAGAA AGAAAGAAAG AAGGAAAGAA 900
GGAAAGAAGG AAAGAAAGAA AGAAGAAAAA AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA 960
GAAAGAAAGA AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA GATGACAGTT CATATGATTG 1020
TGCCTGGTAG TCAGGAAGAC ACCCATAATA GTAAACACTT CTGTCTGGAC ACGGTGGCTC 1080
ACGCCTTTAA TCCCAGCACT TTGGGAGGCT AAGGCGGGTG GATCATGAGG TCAAGAGTTC 1140
GAGACCATCC AGGCCAACAT GATGAAACCC CGTCTCTACT AAAAATACAA AAATTAGCTT 1200
GGTGTGCTGG CGCATGACCG TAATCCCAGC TACTCAGGAG GCTAAGGCAT GAGAATCACT 1260
TGAACCCAGG AGGTGAAGGT TGCTGTGAGC TGAGATCACA CCAGCCTGGT GACAGAGCGA 1320
GACTCCATCT CCAAAAAAAA AAAAAATTAG TTAACCACTT CCTAAGGTTG TTTTGTCCAG 1380
TGTCTGAACA GGGAGGACCC ATGGCAGGTT CTCAAACATC 1420