EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS043-01728 
Organism
Homo sapiens 
Tissue/cell
Fetal_heart 
Coordinate
chr1:67805420-67807820 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1874791chr167806432hg19
TF binding sites/motifs
Number: 31             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:67807104-67807122GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr1:67807108-67807126GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr1:67807133-67807151AGAGGGAGGGAAGGAGGG+6.03
EWSR1-FLI1MA0149.1chr1:67807096-67807114GAAGGAAGGGAAGGAAGG+6.33
EWSR1-FLI1MA0149.1chr1:67807266-67807284AAAAGAAAGGAAGGAAAG+6.33
EWSR1-FLI1MA0149.1chr1:67807145-67807163GGAGGGAAGGAAGGAGAA+6.45
EWSR1-FLI1MA0149.1chr1:67807120-67807138GGAAGGATGGAAGAGAGG+6.54
EWSR1-FLI1MA0149.1chr1:67807270-67807288GAAAGGAAGGAAAGAAAG+7.36
EWSR1-FLI1MA0149.1chr1:67807137-67807155GGAGGGAAGGAGGGAAGG+7.85
EWSR1-FLI1MA0149.1chr1:67807116-67807134GGAAGGAAGGATGGAAGA+8.2
EWSR1-FLI1MA0149.1chr1:67807100-67807118GAAGGGAAGGAAGGAAGG+8.32
EWSR1-FLI1MA0149.1chr1:67807112-67807130GGAAGGAAGGAAGGATGG+9.55
EWSR1-FLI1MA0149.1chr1:67807141-67807159GGAAGGAGGGAAGGAAGG+9.93
IRF1MA0050.2chr1:67807170-67807191ATAGAGAAAGAGAAAGAAGAA-6.88
IRF1MA0050.2chr1:67807155-67807176AAGGAGAAAGAGAAAATAGAG-6
IRF1MA0050.2chr1:67807278-67807299GGAAAGAAAGAGAAAGCAAAA-7.15
IRF1MA0050.2chr1:67807202-67807223AAAAAGAAAGAGAAAGAAAGA-7.64
MEF2AMA0052.3chr1:67805873-67805885ACTATAAATAGC+6.11
MEF2BMA0660.1chr1:67805873-67805885ACTATAAATAGC+6.74
ZNF263MA0528.1chr1:67807125-67807146GATGGAAGAGAGGGAGGGAAG+6.01
ZNF263MA0528.1chr1:67807150-67807171GAAGGAAGGAGAAAGAGAAAA+6.02
ZNF263MA0528.1chr1:67807109-67807130GAAGGAAGGAAGGAAGGATGG+6.04
ZNF263MA0528.1chr1:67805806-67805827ATTTCTTCTTCTTTCTCCTCC-6.25
ZNF263MA0528.1chr1:67807113-67807134GAAGGAAGGAAGGATGGAAGA+6.2
ZNF263MA0528.1chr1:67807096-67807117GAAGGAAGGGAAGGAAGGAAG+6.39
ZNF263MA0528.1chr1:67807093-67807114AAAGAAGGAAGGGAAGGAAGG+6.64
ZNF263MA0528.1chr1:67807121-67807142GAAGGATGGAAGAGAGGGAGG+6.78
ZNF263MA0528.1chr1:67807138-67807159GAGGGAAGGAGGGAAGGAAGG+6.8
ZNF263MA0528.1chr1:67807105-67807126GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr1:67807134-67807155GAGGGAGGGAAGGAGGGAAGG+6.99
ZNF263MA0528.1chr1:67807142-67807163GAAGGAGGGAAGGAAGGAGAA+8.01
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr16780613867806702
Number: 2             
IDChromosomeStartEnd
GH01I067339chr16780513467806903
GH01I067341chr16780735267808340
Enhancer Sequence
ATGAAAAAAC GAGTATCAGA GAGAGGAAAG AGAGGAAGTT CTTGCCCAAA GTCACCCAGC 60
TACTGAGCAC AGACCTGAGA CTGAAACCTT ATCCAGAACT GCTGCATCGT GACTCATCTT 120
TGTTGAAGGA AAATGCTGTG CGATTCGAAT TGAGCTACTG ATTGGCATGC TCATAAGAGG 180
TTTCCTGGTG AACTGCACTC TTTATTTCTC AGGACTCACA TCCTCTTCAC TACACCTCTT 240
CCAGTTGAGG ATAGAAAGTT TTGGAATTAT GAATCTGAAT GAGCACAAAA CCAGAAGAGT 300
AAGAATAACA ATTATAAAGT CCTCTGATGG GGTTCACATG ATGGGTTTTG ATCATTGCAC 360
ACTTCTTCAG TTTTAAGAAA TGAGTGATTT CTTCTTCTTT CTCCTCCCTG TCTCTCTCAC 420
ACACACATAA AACGTCTGGT ATAAGAAGAG ACTACTATAA ATAGCCTGGT GAATCATGAT 480
CAGGCTCTTC ACTTTGAAAC TAACACTGCA GCTCAAAATT TATTTTAAAA TGAATCTACT 540
TTCAATAGCA AGACAATTCT CAAAGCAGGA CATTTAGAAC AGCCATAATT TGTGAATATT 600
ATAGAAGAAC CCAGCCTAAT TATTTCCTTT TCACGAGCAA GTGACTGGTT AAAACCAAAA 660
TTCCTCCTCT CATGTAAAGG TTTCTCCTCC AAAAATGTCC TCAACAGTGA TCTGGAAAGA 720
TATGCTACGT GTTAATCTAT TCCACGCCTC TCAACTCAAG GGTTTCTCTC AGTAGAATGA 780
GGGTAATGAT ACAGGTATCT GCAAAGCTGA CAAGACCATT GTGGGGATCA GCAAATGAGA 840
GGACACAAAT GTAAAAATCA CAAGGGCCAC CAGTGTAAAA TTCAGCAGTG CTGCATGATG 900
CGTGTTTATC CTGACAGTGA AAGCTCCATG CCTGCGTGCT TTTCACTGTA ACAAACAGAG 960
TTTATAGTGG ACATCATCTT GGTTCTCTGA AACCAGCACC AGAGTGAAGT CAAAATAAGT 1020
ATGTGTTGGC CATGAGTGAT GCTTGGTAAA TGTGAGTATG TGATTTCTTC TCTGCTGCCC 1080
TGATTTTATT TCTATCTTCA CAAGGCTTAG GTTCTATAAT GAGGTCTTGG AATTTGGAGG 1140
GACTTCAAAG CTCTTCTAGT TCAGCCTTCC TTTCATTATA AACATGGCTC CTACTCCTGC 1200
CAGGACAGAC AGATGTCTCA GTGGGGATAT TCTGGGACAG GGAGAATCTC ACTTTGTAGT 1260
CTGCCCATGC CATGGTTGAA CATCTCTTAT TGTTTAGAAA ATGTTTCCTT TTGTGTAGCC 1320
AGAATTGTGG GCCCAAGAAG GATGCTTGGG GTTGGAACTG GCTTAGAAGA AACCAAAAAG 1380
GGCAAGGCAC AGTGGCTTAC GCCAGTAATA ATCCCATAAT CCCTAATCCC AGCACCTGGG 1440
GAGGTCGAGG TGGGCAGATC ACTGAAGTCC AGGAGTTTGA GACCATCCTG GCAGACATGG 1500
TGAAACCCTG TCTCTACCAA AATACAAAAA AATCAGCTGG GTGTGGTGAT GCCCACCTGT 1560
AATCTCAGCT ACTTGGGAGA CTGAAGCAGG AGAATCCCTT GAACCCGGGA GGCAGAGGTT 1620
GCAGTGAGCT GAGATCGTGC CATAGTACTC CAGCCTGGGT GACAGAGCAA GACAAAGAAG 1680
GAAGGGAAGG AAGGAAGGAA GGAAGGATGG AAGAGAGGGA GGGAAGGAGG GAAGGAAGGA 1740
GAAAGAGAAA ATAGAGAAAG AGAAAGAAGA AAGAAGGAAA GAAAAAAGAA AGAGAAAGAA 1800
AGAAAGAAAG AAAGAAAGAA AGAAAGAAAG AAAGAAAGAA AGAAAGAAAA GAAAGGAAGG 1860
AAAGAAAGAG AAAGCAAAAA GGTAAGCACT AGAAGCTTCT ATAACTTGAT GTCAGATGGT 1920
AGTCATCAAA AGCCAACCTC AAAACCTTCA GTGACTCTCT AGTCTAAGAG GCTCCCCAAG 1980
GAAAGTTGGA TGCAGTCCTA TATTGTCACA GGATTAAGTC CTTTTCTGTC AAACCTGGGC 2040
TTCTTTAATG GCCCCAAACA GGCCACTCAA CTGAGGGTGG GAATGGAAAC ACTGACCAGA 2100
GTTACTGAGC AGTCCTGCTT TGGACCACAG AACCACAGAG TTATAGACCT CTAGAGCCAA 2160
AGGGATTTAA CTGTCATGTA GTCTCACCCC ACAGTTTAAA ACATGGAAAC TGAGGTTTCA 2220
AGAGGTGATT TTCCAGTGAG GGGATTTCAG GTGATTTGAG TCCACTCTTA TCCCAGCCTC 2280
TAATAGGGAT TCCTCATGCC ACTCTCAGGC AGGCTTGGGA ATTCAAGGGA ATGCTGTGGT 2340
ACAAGGGAGT TATCTAAGTG TCAGGCTAGA AGGAAAACTC TGCAGCCAGA TCGCTTTGTG 2400