EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS129-10472 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr13:50215500-50216930 
Target genes
Number: 8             
NameEnsembl ID
TF binding sites/motifs
Number: 54             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr13:50216535-50216553GGAAGGAAGGCAGGAAGG+10.35
EWSR1-FLI1MA0149.1chr13:50216560-50216578GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr13:50216564-50216582GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr13:50216601-50216619GAGAGTGAGGAAGGAAGG+6.14
EWSR1-FLI1MA0149.1chr13:50216523-50216541GAGAAGAGGGAAGGAAGG+6.22
EWSR1-FLI1MA0149.1chr13:50216568-50216586GGAGGGAGGGAGGGAAAG+6.31
EWSR1-FLI1MA0149.1chr13:50216693-50216711GAATGGAAGGAAGGGAGG+6.68
EWSR1-FLI1MA0149.1chr13:50216555-50216573GGAAGGGAGGGAGGGAGG+7.08
EWSR1-FLI1MA0149.1chr13:50216733-50216751GGAAGGGAGGGAGGGAGG+7.08
EWSR1-FLI1MA0149.1chr13:50216527-50216545AGAGGGAAGGAAGGAAGG+7.85
EWSR1-FLI1MA0149.1chr13:50216705-50216723GGGAGGAAAGAAGGAAGG+7.87
EWSR1-FLI1MA0149.1chr13:50216605-50216623GTGAGGAAGGAAGGAAGG+7.88
EWSR1-FLI1MA0149.1chr13:50216709-50216727GGAAAGAAGGAAGGGAGG+7.93
EWSR1-FLI1MA0149.1chr13:50216701-50216719GGAAGGGAGGAAAGAAGG+7.95
EWSR1-FLI1MA0149.1chr13:50216713-50216731AGAAGGAAGGGAGGAAGG+8.05
EWSR1-FLI1MA0149.1chr13:50216551-50216569GGAAGGAAGGGAGGGAGG+8.13
EWSR1-FLI1MA0149.1chr13:50216729-50216747GGAAGGAAGGGAGGGAGG+8.13
EWSR1-FLI1MA0149.1chr13:50216609-50216627GGAAGGAAGGAAGGAGAG+8.99
EWSR1-FLI1MA0149.1chr13:50216697-50216715GGAAGGAAGGGAGGAAAG+9.01
EWSR1-FLI1MA0149.1chr13:50216543-50216561GGCAGGAAGGAAGGAAGG+9.17
EWSR1-FLI1MA0149.1chr13:50216539-50216557GGAAGGCAGGAAGGAAGG+9.25
EWSR1-FLI1MA0149.1chr13:50216547-50216565GGAAGGAAGGAAGGGAGG+9.42
EWSR1-FLI1MA0149.1chr13:50216725-50216743GGAAGGAAGGAAGGGAGG+9.42
EWSR1-FLI1MA0149.1chr13:50216721-50216739GGGAGGAAGGAAGGAAGG+9.47
EWSR1-FLI1MA0149.1chr13:50216717-50216735GGAAGGGAGGAAGGAAGG+9.6
EWSR1-FLI1MA0149.1chr13:50216531-50216549GGAAGGAAGGAAGGCAGG+9.99
IRF1MA0050.2chr13:50216660-50216681AAAAGGAAAGAAAAAGAGAAA-6.32
IRF1MA0050.2chr13:50216666-50216687AAAGAAAAAGAGAAAGAAAGA-7
ZNF263MA0528.1chr13:50216614-50216635GAAGGAAGGAGAGAGAAAGAA+6.03
ZNF263MA0528.1chr13:50216591-50216612GAGGGAAGGAGAGAGTGAGGA+6.04
ZNF263MA0528.1chr13:50216595-50216616GAAGGAGAGAGTGAGGAAGGA+6.11
ZNF263MA0528.1chr13:50216610-50216631GAAGGAAGGAAGGAGAGAGAA+6.12
ZNF263MA0528.1chr13:50216606-50216627TGAGGAAGGAAGGAAGGAGAG+6.18
ZNF263MA0528.1chr13:50216706-50216727GGAGGAAAGAAGGAAGGGAGG+6.18
ZNF263MA0528.1chr13:50216711-50216732AAAGAAGGAAGGGAGGAAGGA+6.1
ZNF263MA0528.1chr13:50216506-50216527GGAGAAGGAGAAAAGAGGAGA+6.24
ZNF263MA0528.1chr13:50216519-50216540AGAGGAGAAGAGGGAAGGAAG+6.24
ZNF263MA0528.1chr13:50216719-50216740AAGGGAGGAAGGAAGGAAGGG+6.2
ZNF263MA0528.1chr13:50216536-50216557GAAGGAAGGCAGGAAGGAAGG+6.33
ZNF263MA0528.1chr13:50216723-50216744GAGGAAGGAAGGAAGGGAGGG+6.36
ZNF263MA0528.1chr13:50216532-50216553GAAGGAAGGAAGGCAGGAAGG+6.46
ZNF263MA0528.1chr13:50216509-50216530GAAGGAGAAAAGAGGAGAAGA+6.49
ZNF263MA0528.1chr13:50216503-50216524GAAGGAGAAGGAGAAAAGAGG+6.53
ZNF263MA0528.1chr13:50216698-50216719GAAGGAAGGGAGGAAAGAAGG+6.62
ZNF263MA0528.1chr13:50216557-50216578AAGGGAGGGAGGGAGGGAGGG+7.05
ZNF263MA0528.1chr13:50216565-50216586GAGGGAGGGAGGGAGGGAAAG+7.12
ZNF263MA0528.1chr13:50216714-50216735GAAGGAAGGGAGGAAGGAAGG+7.12
ZNF263MA0528.1chr13:50216548-50216569GAAGGAAGGAAGGGAGGGAGG+7.19
ZNF263MA0528.1chr13:50216726-50216747GAAGGAAGGAAGGGAGGGAGG+7.19
ZNF263MA0528.1chr13:50216722-50216743GGAGGAAGGAAGGAAGGGAGG+7.22
ZNF263MA0528.1chr13:50216569-50216590GAGGGAGGGAGGGAAAGAGAA+7.28
ZNF263MA0528.1chr13:50216552-50216573GAAGGAAGGGAGGGAGGGAGG+7.38
ZNF263MA0528.1chr13:50216730-50216751GAAGGAAGGGAGGGAGGGAGG+7.38
ZNF263MA0528.1chr13:50216561-50216582GAGGGAGGGAGGGAGGGAGGG+7.97
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr135021618550216584
chr135021590850216514
Number: 1             
IDChromosomeStartEnd
GH13I049640chr135021511250218336
Enhancer Sequence
AAAGGGCGGG ACCTTCACAG CTTTGCCTAA GGCCATTATG AATTTGGACC AAATAGGTAT 60
TATCATCCAC ACAGGCAGGA CCTCCTGGGT AGGGGGCTGC CACCTTTTCC AGGCACTTGG 120
AAGGGTGGCC TCCAGCTGTG GAGCCACAGA ACTAAATATT ATAGCTGGCC CAGGAGCACC 180
CGTTTAGGCT AGGGAAGGAA TAATAATCCG GCTTCTCCTT CCTCTGACCC TGAGATTTCG 240
GCCAAGTCTC CATTAGAGAT TGGCCTCCTA GAGTGTAAAA CAGGGTGGAC AAGTTTGGAG 300
AATGGATCTG GGATGGGGTG GGGAATGGCA AATGGAAAAA AGGCAGCACA AACTCTTTAT 360
TGTCATTCAG AGAATGCTGA GGTCCAAGGC ACAACCAGCC AGAGGGTTGC TTCAGCCTTT 420
CACTGGAAAA GCCACATTTT CCTCAGTTGT ATCCTCACTT CGAGTGAGGC TTCTCCAAAT 480
GCAGAAGGAC AGCATCATGA CCCAGGCCGA GAAAGTATGA TTGCAAAATT CCATGGGCCT 540
AACCCTAGTG GGGGAGGGAA TCCATTCTTT TAAGCCAGGG TTTAAAACTC TTCAAGCAAG 600
TCATCTGCAA AGGTACCGCT TCTACCATTT TAAAGATAGG ATTATGTTCC CTAGGACAAC 660
TGGATGAGCC CTAGGAACCA AGAACCCTGT GCAGCTGGGG CAGAAGCCTG AGGGTTCCTT 720
TGTTCCCCCA CAGCTGTAGG TCACAAGGTT CTTACACAAG CTTTGGGGTG GCCCCACCCC 780
ACACCCTTCC TTCCCCTCAG TCAGTGATGA CTCAAGAGGT TTTGGGAAGG AGCTCAGGGA 840
ACACTCAAGC AGCAGGCTCA GCTTACGGCA CTTCTGATGC ATTTTCTAGA TAACATTAGT 900
TGCTGGTTCC AGACAGGACT CAGAAGTATG GACATTCACT CCCCAGGCTT GGTCATCAGT 960
GCCCTGTGAG TTCAGGAATA CACTACCTAA AGGAGATCTT TAGGAAGGAG AAGGAGAAAA 1020
GAGGAGAAGA GGGAAGGAAG GAAGGCAGGA AGGAAGGAAG GGAGGGAGGG AGGGAGGGAG 1080
GGAAAGAGAA AGAGGGAAGG AGAGAGTGAG GAAGGAAGGA AGGAGAGAGA AAGAAGAAAG 1140
AAAGAAATAG AGAAAGCAAG AAAAGGAAAG AAAAAGAGAA AGAAAGAAAG AGAGAATGGA 1200
AGGAAGGGAG GAAAGAAGGA AGGGAGGAAG GAAGGAAGGG AGGGAGGGAG GGAGCTGGCC 1260
GGACGTGGTG GCTCATGTCT GCAATCCCAG CACTTTGGGA GGCCGAGGCA GGTGGATCAC 1320
CTGCAGTCAG GAATTCAAGA CCAGCCTGGT CTACATGGCG AAACCCTGTG TCTACTAAAA 1380
AAATAAAATT AGCTGGACGT GGTGGCAGAT GCCTATAATT CCACTTACTT 1430