EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS092-14678 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr13:50215410-50217040 
Target genes
Number: 9             
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
CAGCCCTTTT CAGGACAGCG TTTGTGAGGC AGCAAAGCTA AATGTTGAGA AGGGCCTGAA 60
AGAATGATGG ACTGACGCTG CCAAAAAGAG AAAGGGCGGG ACCTTCACAG CTTTGCCTAA 120
GGCCATTATG AATTTGGACC AAATAGGTAT TATCATCCAC ACAGGCAGGA CCTCCTGGGT 180
AGGGGGCTGC CACCTTTTCC AGGCACTTGG AAGGGTGGCC TCCAGCTGTG GAGCCACAGA 240
ACTAAATATT ATAGCTGGCC CAGGAGCACC CGTTTAGGCT AGGGAAGGAA TAATAATCCG 300
GCTTCTCCTT CCTCTGACCC TGAGATTTCG GCCAAGTCTC CATTAGAGAT TGGCCTCCTA 360
GAGTGTAAAA CAGGGTGGAC AAGTTTGGAG AATGGATCTG GGATGGGGTG GGGAATGGCA 420
AATGGAAAAA AGGCAGCACA AACTCTTTAT TGTCATTCAG AGAATGCTGA GGTCCAAGGC 480
ACAACCAGCC AGAGGGTTGC TTCAGCCTTT CACTGGAAAA GCCACATTTT CCTCAGTTGT 540
ATCCTCACTT CGAGTGAGGC TTCTCCAAAT GCAGAAGGAC AGCATCATGA CCCAGGCCGA 600
GAAAGTATGA TTGCAAAATT CCATGGGCCT AACCCTAGTG GGGGAGGGAA TCCATTCTTT 660
TAAGCCAGGG TTTAAAACTC TTCAAGCAAG TCATCTGCAA AGGTACCGCT TCTACCATTT 720
TAAAGATAGG ATTATGTTCC CTAGGACAAC TGGATGAGCC CTAGGAACCA AGAACCCTGT 780
GCAGCTGGGG CAGAAGCCTG AGGGTTCCTT TGTTCCCCCA CAGCTGTAGG TCACAAGGTT 840
CTTACACAAG CTTTGGGGTG GCCCCACCCC ACACCCTTCC TTCCCCTCAG TCAGTGATGA 900
CTCAAGAGGT TTTGGGAAGG AGCTCAGGGA ACACTCAAGC AGCAGGCTCA GCTTACGGCA 960
CTTCTGATGC ATTTTCTAGA TAACATTAGT TGCTGGTTCC AGACAGGACT CAGAAGTATG 1020
GACATTCACT CCCCAGGCTT GGTCATCAGT GCCCTGTGAG TTCAGGAATA CACTACCTAA 1080
AGGAGATCTT TAGGAAGGAG AAGGAGAAAA GAGGAGAAGA GGGAAGGAAG GAAGGCAGGA 1140
AGGAAGGAAG GGAGGGAGGG AGGGAGGGAG GGAAAGAGAA AGAGGGAAGG AGAGAGTGAG 1200
GAAGGAAGGA AGGAGAGAGA AAGAAGAAAG AAAGAAATAG AGAAAGCAAG AAAAGGAAAG 1260
AAAAAGAGAA AGAAAGAAAG AGAGAATGGA AGGAAGGGAG GAAAGAAGGA AGGGAGGAAG 1320
GAAGGAAGGG AGGGAGGGAG GGAGCTGGCC GGACGTGGTG GCTCATGTCT GCAATCCCAG 1380
CACTTTGGGA GGCCGAGGCA GGTGGATCAC CTGCAGTCAG GAATTCAAGA CCAGCCTGGT 1440
CTACATGGCG AAACCCTGTG TCTACTAAAA AAATAAAATT AGCTGGACGT GGTGGCAGAT 1500
GCCTATAATT CCACTTACTT GGGAAGCTGA GGCCAGAGAA TGGCCTGAAC CCGGGAGGCG 1560
GAGGTTGTGG TGAGCCAAGC TCGCGCTACT GCACTCCATC CTGGGCGACA GGGCGAGACT 1620
TCATCTCAAA 1630