EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-05471 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr1:230960160-230964480 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs78977568chr1230963730hg19
TF binding sites/motifs
Number: 18             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EBF1MA0154.3chr1:230961520-230961534AATCCCAAGGGATT-6.04
EBF1MA0154.3chr1:230961520-230961534AATCCCAAGGGATT+6.34
FOSL1MA0477.1chr1:230960870-230960881CATGAGTCACC-6.62
JUN(var.2)MA0489.1chr1:230960400-230960414ATGACTCACCTTCT-6.51
JUNDMA0491.1chr1:230960870-230960881CATGAGTCACC-6.02
MEF2AMA0052.3chr1:230960856-230960868TCTAAAAATAGC+6.52
MEF2BMA0660.1chr1:230960856-230960868TCTAAAAATAGC+6.22
MEF2CMA0497.1chr1:230960854-230960869AATCTAAAAATAGCT+7.11
MSCMA0665.1chr1:230962413-230962423AACAGCTGTT+6.02
MSCMA0665.1chr1:230962413-230962423AACAGCTGTT-6.02
MYCNMA0104.4chr1:230962940-230962952GGCCACGTGGTC+6.52
MYCNMA0104.4chr1:230962940-230962952GGCCACGTGGTC-6.52
MYF6MA0667.1chr1:230962413-230962423AACAGCTGTT+6.02
MYF6MA0667.1chr1:230962413-230962423AACAGCTGTT-6.02
Myod1MA0499.1chr1:230961073-230961086TGCAGCTGTCACC+6.5
MyogMA0500.1chr1:230963356-230963367CTGCAGCTGTT-6.02
TFAP4MA0691.1chr1:230961672-230961682ATCAGCTGTT-6.02
Tcf12MA0521.1chr1:230963356-230963367CTGCAGCTGTT-6.62
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_01660chr1:230958602-230964574Aorta
SE_03178chr1:230958859-230964538Brain_Angular_Gyrus
SE_03954chr1:230955295-230964726Brain_Anterior_Caudate
SE_04839chr1:230953828-230965559Brain_Cingulate_Gyrus
SE_05854chr1:230953745-230964911Brain_Hippocampus_Middle
SE_06754chr1:230953876-230964871Brain_Hippocampus_Middle_150
SE_07794chr1:230953717-230964874Brain_Inferior_Temporal_Lobe
SE_30437chr1:230956195-230964508Fetal_Muscle
SE_36964chr1:230959481-230965031HSMMtube
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1230962853230963636
Number: 1             
IDChromosomeStartEnd
GH01I230820chr1230956320230964560
Enhancer Sequence
CCTCAAGGTC TCATCTCCAC CAGGCCACAG GGTCCCAAAA AAGTCACATA GTAAACAGAA 60
GGGGTATTTT TCAGGCCCAA ATTATAGCCT GAACTAAACT AATGAAACCG GCTTATTAGG 120
TCAACTGTAT TCACTGGGGG AATAATGTTC TTTTTTCTCC AACTATACTA CCTATGAAAT 180
TCCTCTTCCC TTCTTTGGAC AATATCTCCA CCATTCCCTA AGGCCTTCTT CTTAAGGGCA 240
ATGACTCACC TTCTGGCACT AAATGTCCAG CTCAGGCCCA GCTAGCTTCT GGGTGTCCAG 300
TTTGCACTCC AGGCGGTGGA CGGGCCAGGG GCTCCCACCA TGGTCTCTCT TGCTGCCCTG 360
CCATGGAGAC AGCCCCAGAT AGCCCCCCAC ATCATAAGGG GTTTTCAAGG ATGTGCAGAG 420
GGAGGACATA CATTGCCAGA GCCACCTGGA AGCGGTGAAG CCAGCAGAAG TGATGCCTAC 480
CAGGTGCCAG ACGCTGCTCC AGAGACCAGA CATTCTGCAA GCCTGCCAGA GCCTTGACTC 540
TCAAGGAGCT CGTAGTCTAA TGGACATGCG AGTGAAGGAT GCTTTCATCT GGCAGCAAGA 600
AGGTGAATGT GCTTTGTAAA ATGACTCAAT TATTAAGATC ATAGAGAGCA GAGACGGTTA 660
TATATGTCGA TTTTTATTAC AGTTTAATCT AGAAAATCTA AAAATAGCTA CATGAGTCAC 720
CAGTCAGGAG ATGTGTTTCA GGGTAGATGG CAGTTTGCTG AGCAAAGAAC CAGGAGGCTA 780
TGGGGAGAAA GGACATGTTG TAACCCTAGT GCCTGGAGGG CACTAAACCT CTATCCCTGC 840
TTCTGATTCG CATTTGCTAC ATGAGACAGA CACTGATACA ACAAAACTGT AAGCAACTCT 900
CCAAGCTATA GGATGCAGCT GTCACCGAGT TTCAGGGGAA GGAAAGGGCA CCAGAGTTTG 960
CTTTCGGGCT GCTTTGATAA TGAGTTCCCT GATAATGACA AACAACACAG GTTAGGTTTC 1020
TGCTCTGTGC CAGTCTCTGT TGACTGTGCT TGGCAGTGTT ATTCCTTTTG TCCTCATACC 1080
AACCGTATGA CATAAAACTA TTGTTTTACT CATATTACAG ATGAGGAACT TGGGAAAGAG 1140
AAAAGTTAAG TAACATGTCT TATGTGACTT ACTAATAAGA AGGCACTTAG AAACGGAAAC 1200
TCTTTCCTAG GGGTAATTGA AGCAATTTGT AATTGTGCCC CTGACGGGAC ATAACCAATG 1260
GGTAGGGGAG GATTTTCGTG AGTGGTCCAG TTCTAGAAAG CAGGTCTTTC ATGTAATAGC 1320
ACATTTTCCT AAATGGCATT ACAAAAGTGG CTGTGGCTAG AATCCCAAGG GATTTGGGAT 1380
TCTGGCAATG AGGAGAAGTG GAGAGAAACT GTCCAAAGTG CAGGCTATTT ATTGATCACA 1440
GAAACCCTGC GTCAGTGCTG ACTGAGTCTG GGATGCAGGC TGATGCAAGG AGAGTGAGTG 1500
ATTCTGGGAG AAATCAGCTG TTCTGCCTGC CTCCCATGGG GCCCTAAAAC TGCACCGTCT 1560
GCCTCAGTGC ACTACCAGTG CAAGAGCCCC TGTTGGAGGA GGGAGGGCAA AGGCCCTGGG 1620
GAGAGCAGAG CTGGATATGC AAGGGCTGGA AGACAGAAAC CAGTGTACGC AGGGCTGGTC 1680
TGCCAGAAGC AACATTGGGC ACCTGCTTCT CCAGCTGCCC AAGGCCAGGA GGGCTTCTCA 1740
ACCACTGTCC TCATCCACTA CCCCTGCTCT GGTGCTGCCA GGCACAGAAT GCACCTGGAG 1800
GAAGAGCTGA GTAGAACGAG AGCTGGAGGG TGGGAGCTGC GTGTTGGAGG GAAGTTGAGT 1860
ATGACTTAGG TCCAGGCACT CGACACCCCC TCTATGGAGT CAGCCCTCGG GGAGTCAGAA 1920
AAACAGAGGT AGCCAATCCC ACTGCAGGGA GCTGGCAGAG TCAGGTGGCA TGCAGGAGGA 1980
AGCAGGAGAA AGAGCACAGC AAGAGGGGCC TGGAAATGGG AGCAAAGTCA TCAAAGGCAC 2040
GGCACCCTCT TCAGTGGACG GGCATGGCCT CAGAGGTGGT GGCAAGGAAG GAGGACAGGA 2100
GTCTGGCTAG CTGTGTAGAA GCCTTTTGGG GCACCGGGAC AGGGAGCCAC CTTCTGCCCC 2160
CTCACCTCCA GCTTCCCCCG ATTCATTGTG CAACTGCTGA TAAAATAATG GCTGTCATTG 2220
ATGGCATGCT TATTGCGTGC CAGGCATTAT GTTAACAGCT GTTTTATTCA ATCCTCTCAG 2280
CAACCCTGTG AGGTTGAGAG AGATAATAGA ATCCATCACA TCACATGGCT GGGAAGGAAT 2340
CTCAGTCTGT GCAACTCAAA GTCCATTCTT AATCCCCAAC CCTCCTGCAC ACCCTCACCT 2400
GAAGCTCCCC AAGCCAAGAC TAGAGGTGCT ATCCAGGAGG GTCCCACAAG CAACTGAAGA 2460
TCTGAGACCC CTGTGTTCTT AATCTTGTGC TCCAGAAGGA ATGAGAGCTG AGTGTGGAGG 2520
AGGCATACAC CGTGCCAAGG CCCCTGGAGC TCAGATCTAA GATTCAAGAT GTGTAGGGCC 2580
CAGGCACTCT TTGGTCACTG AGGCTGGGTC ACCCCTCCTG CCACTCCCTG CGTCTTCCCC 2640
ATCCACGGCC CCACTCCTAC CCCAACTGTG AGCAGTCAGT GATGCTCTTT TAGAAACCAC 2700
ACTACACAGA ATGTGGCTGT TTTCTGGATG GCTTCAACCT GCTATCCAAC AACAATCAAA 2760
CCCACATCAC GCTCTGGCAA GGCCACGTGG TCCTCCAGGC CCTGAAACTG GCACAGTCAG 2820
CGGCCAGCAC TGCCATTAGA CATGGGAGAA GCTGAGTACA GCATAAGGCC TGAACCTACC 2880
ACAGGGAAGT CATCTCACCC AGGAAAAGGA CTTCTGACCC CCAAAGCAGA GAATGTGCCC 2940
AACCTATCTG TGGTTAGGAG ACAACTCATT CATTGAATAA GAACTCATTC ATTGAACTCA 3000
TTCATGTGAA AGTCACGGCC ACTCATCTGT GCACCATGTC TCTGAAGAGG CCCCTGGATC 3060
TGGGCAGCAG CCAGCCTGTC CACCCCCTCC CCACGGGCTG CTCTCGGCCA GCTGTTCCGT 3120
CTCTCCTCCT GTGTACAGCC CTGCCTTTTC ACCTCACTGG CCTTGCCCCT CTGGCCCTGG 3180
GATGCTGCTC TTGGCTCTGC AGCTGTTTGG CTGGATGCCT CTGAATAGAA CATTCAGCCT 3240
CTATGTTCTT CTATTTCTTC AACTGGAAAA CAGAGAGAAA TATGGTCATC ATTTTTTTTC 3300
AAGGGGTAAA GGAGTCATTG GAAGGAATAG CCTGGTAAAG ATTCAAAACC CATCGGCTAT 3360
TTGGAAGAAA AGTTGCTGCA TAAATAAGCT GCTTGACCCA AGGCCCATTT TGTACGCTTC 3420
TTTGAGGTCA ATCTTGTTTA TTTTCCTGGC TCACAATCCC CAAAGGTTGG GGTGGGCCAA 3480
AAGGCAAACC TGCCCTTTGC AGGGGCCTCT CCTGTCAAAT TAATCTGATG ACTTGATGGA 3540
GCAGTGGGTG GAAGAGAACA TGGCCCCGTA AGGTTAGCGG TGGAATCCCT GCTGGAGAGA 3600
AATGACGCTG GCCCAGGGGG GATGTGCCTT GTGCCCAGCC TGGACAGGCC AGTTCACTTC 3660
TCGGGGCATA GGCTCTCCCT TCCTCCTCAT GAGAATAAGA ACACCAACTC TACTCCCTGA 3720
CAGTCTCCTA ACTTGGTCTC CTGAGAACTC AGTGAGGCTG GCAGGGAAGG GATGATTATA 3780
TCTGTGTTAC AGAGAAGAAA ACAGACCTAT TCAAAGTCAC AGAAATAAGT GGGGACAAGA 3840
CCTTAGTCTT CTGCCTACGT GACTCATTTT CATACAATAC ATACCTTAAC CCTAACATAG 3900
AGCCGTGATA CAAGTCAAAT GAAAGAATGT ACAGAAGGCC TTCCGAAAGG GGGTGAAGCT 3960
CTGTGCAGTG CTGTCCAGCA AAAATAAATG CAAGTCACAT AATGTGATTT TTGTCACTTA 4020
TGTGCAACCA CATTTAAAGT GTAAAAAGAA ACAAATGGCA GGGCGTACCT CCTGCCAAGC 4080
TACTCCTAAG CTAGGGCAGC TAGGAGGATC CACAAGGCCT ACTCGAAGGA GCTGGAGAAC 4140
TGCTCAGGGA CAAAGAACAA GAACAATGGA AGCAACTCGA ACACTTTCAC TGCCCAGGGG 4200
TCTTCCACCT TTATTTATGT CTTTTCACCA GAACCTTAAT TGGATGCAAA CCCTCAATGT 4260
AGGAAACAAA TGAACCCAGA GCTCTCCAGT GGAAGGGCTC AGACCAGCCA ACAGGCCTCT 4320