EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS043-20675 
Organism
Homo sapiens 
Tissue/cell
Fetal_heart 
Coordinate
chr19:18228050-18231070 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10401175chr1918230274hg19
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EGR1MA0162.3chr19:18228781-18228795CCCGCCCCCGCACT+6.21
EGR3MA0732.1chr19:18228780-18228795CCCCGCCCCCGCACT+6.83
EGR4MA0733.1chr19:18228780-18228796CCCCGCCCCCGCACTC+6.16
INSM1MA0155.1chr19:18228093-18228105CGCCCCCTTACA-6.37
IRF1MA0050.2chr19:18230233-18230254TGTGGGTTTCACTTTTGCTTC+6.67
KLF14MA0740.1chr19:18228423-18228437GGGTGGGCGTGGTA-6.08
KLF16MA0741.1chr19:18228599-18228610GCCCCGCCCCC+6.02
KLF16MA0741.1chr19:18228764-18228775GCCCCGCCCCC+6.02
KLF16MA0741.1chr19:18228779-18228790GCCCCGCCCCC+6.02
KLF5MA0599.1chr19:18228599-18228609GCCCCGCCCC+6.02
KLF5MA0599.1chr19:18228764-18228774GCCCCGCCCC+6.02
KLF5MA0599.1chr19:18228779-18228789GCCCCGCCCC+6.02
SP1MA0079.4chr19:18228761-18228776CAGGCCCCGCCCCCA+6.56
SP3MA0746.2chr19:18228424-18228437GGTGGGCGTGGTA-6.37
SP4MA0685.1chr19:18228761-18228778CAGGCCCCGCCCCCAAC+6.57
SP8MA0747.1chr19:18228424-18228436GGTGGGCGTGGT-6.32
ZfxMA0146.2chr19:18228761-18228775CAGGCCCCGCCCCC-6.19
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_03607chr19:18228860-18229540Brain_Angular_Gyrus
SE_03607chr19:18229563-18230152Brain_Angular_Gyrus
SE_04405chr19:18227552-18228448Brain_Anterior_Caudate
SE_04405chr19:18228707-18231550Brain_Anterior_Caudate
SE_05422chr19:18228732-18231107Brain_Cingulate_Gyrus
SE_06334chr19:18227733-18231497Brain_Hippocampus_Middle
SE_07235chr19:18227822-18231343Brain_Hippocampus_Middle_150
SE_08343chr19:18228675-18231084Brain_Inferior_Temporal_Lobe
SE_10753chr19:18227967-18228613CD19_Primary
SE_10753chr19:18228829-18231042CD19_Primary
SE_19731chr19:18227880-18228741CD4p_CD25-_Il17p_PMAstim_Th17
SE_19731chr19:18228750-18231627CD4p_CD25-_Il17p_PMAstim_Th17
SE_22919chr19:18227678-18228683CD8_primiary
SE_22919chr19:18228828-18231785CD8_primiary
SE_60731chr19:18199190-18231325DHL6
SE_62682chr19:18196873-18231497Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr191823004418230277
chr191822859718228694
Number: 1             
IDChromosomeStartEnd
GH19I018117chr191822801118232079
Enhancer Sequence
AATTATATAT AGATATGGAA CATATACCAG GTGCCCTTGG AAGCGCCCCC TTACATCTGA 60
TTTGTGTAAT TCTCATGTCA GTTCAGTTTT CCTCCAATTT CACAGTTGAG GAGACTGAGG 120
CTGGAGTTCA ATCAGGTGGC TGCTTCCTAA CTGAGGCAGG GCTGATGGCC TTTCCCGCCA 180
CACACAGACA GAGCATGTCA GACGCCCCGA CTCAATTTGC CAAACACACC CTCTATGCCA 240
GTCCGGTGCT GGGAGCTGCT GGGACCCTAA GGAGCCCCCA GCCTGGGGAA GACATAGCCG 300
GACAGACAGG AAAGCGGGTT TTTCAGAGGA GAGGACGCAG TTTTGCCAGG CTAGATTCCA 360
AGCAGTGGGG CCAGGGTGGG CGTGGTAGCA TGAGCCGGCC AGGACGCTGG GGTGGGTCTT 420
GGGTGCCGCA CTGAGAAGGG GTCAGTGCTC TGGGAGAGAG GAAAAAGATG GAGGGAGCGA 480
TTAGATTTAC ATTTTAGCAG AAAGGAGCCA AAATGCCTGC CCCTAGCTCG AGGTTAAGGT 540
GCTGCCAACG CCCCGCCCCC GCCGCCCGCG GTCGTAGCAA CGCCCGGCCT CAGCCGCCCG 600
CGGCCCTAGC AACGCTCCGC CTCTCCGCCC GCGGCCATGG CAGCGCCCCG CCCACTCGCC 660
GGCACGCGGG TCCGCCGGCC TCGCTTCCGC GTCGCTCGCT CCGCCTCCCG ACAGGCCCCG 720
CCCCCAACGG CCCCGCCCCC GCACTCGCCT GGGCGGAGTT CCAGTCGCGC TCGGGGGCGC 780
GCGCTTCCTT CTCGCCGCCC CCCCATCCCC GCAGCCCCGT GCGCCCCCCT CCCTGTCCGG 840
CTCCGCGGGG CTCCTGGGGC CGATCCCACC GCCGAGGCCT CCCTTCCCGG CCTCGGGCGG 900
CTGCGGCGGC ACAAAGGGAA GCAGCATGTC CGACCCCAGC TACTGGACGG CGGTGGCGGC 960
TCCCGGCCAT CGGAGCCGCC TGGCAAAAGG CGCGCTGCTG CAGCGCTCCA AGAGGTAGGG 1020
GGCACGGCGC CGGCGAAGGC TCGGCGGCCA GCCGAGCAAA CAGGAGTTGC CAGAAGTGTG 1080
TCCTGGCCGC GTGGCGCGGA CCACGGCGAG CGTCTGTCTG TGGCAGCAGT GGGAAGGGGG 1140
GAGGACGCCT GTGGATCGAG GTGTCCCCTG GGGTCCCTGG CACCCTCCTT TCGCCCCTCG 1200
TTCCCTGGAC TGGGGTGTCT GTCCGCCAGC GTCGCAGCTG GGGTGGTGAC AGACAGGAGT 1260
GAGTTGAGAT TGAGCTAGGA TTTGAACCCG GGTGTCCAGG GCTGGGCAGA ACCAGGGAGG 1320
AACTTCTTGG AAAAACTGAG GCTGATCTGC CGCTGGGGGT CCATTCAGCA GAAATGTTGG 1380
CTCAGAAGCA AATATTTACT GCACGAGGCT GGCATTTGGG TGGGGTGTCA GGAGTCCAGA 1440
TAGTTGGGGT TAACCCCCGC CAAAGCCTCA CCGCTCTTGG AGTCTCAGTT TCCCCTTTTG 1500
AAAAGCAGAG AGGATAAGTG AGGGCTGTGG ATTCTACCAG ACCTGGGTTC AAATTTCGAC 1560
TCAGCCACTA CCAGGCTGTG TGACCTCAAG TAGCTCCTTA ACCTCTCTGT GCTTGGGTTT 1620
CTCATTGGTG CTGGACTGGG GCAAAGTCTG GGCGGTGGGA CCAGCTACCG AAAGACCTTG 1680
AATGCTGAGT CCAGGGCTTA AACTTACCTC CAAGATCGTG GGGAGCATTG GAGGGGGAAT 1740
ATGGGTGCCA GAGGGATGAG GTGCAGGAGG CTGGCTTCAG GCCCCTGCTT TCTGCCACAT 1800
TCTCTCTGTT GTGTCCTGGG TACCAAGAGA GGATCGTTCT CAAATGGCAA CTTCTCGAGG 1860
TCCTGGATCT CCTCCAGGAA GAGTTGAACA AACAGTCGGC CCTGCATAGA TGCTTGGGAA 1920
GTGAACAGAT GATGCTTAGT TCTCCTTTGA GGCCTCACAT TTGGCCGTGT TTTCAAGAAG 1980
ACCTCGCCCA AGAACAGGAG GGAGGGCAAC GAAGTGTTTT TCCCAAATGC TTTTGGAAGC 2040
AGCAAGTGAT ACAGCAGGAT CGGGGAGGGA GGGTGCTGGT GGTGCAGTGT GGGGGCGAGG 2100
AACCAGGTGA GGGGCTGGGA GAGGATGTGG AGACAGCCAG GTGAGCGTGC ATTGAGGGGT 2160
TGGCAGGAAG TTTTGCAGAA ACCTGTGGGT TTCACTTTTG CTTCTGCAGC TCAGGCTGGG 2220
AGACAATCAC TGTGACTGTT GACATCTGTG GCTTCAGTTT CCCAGTCTGG AAAATGGGCT 2280
CAGCTGGTCA TTCCCAACTC TGGGGCTTGT TGGAATTGGC AGATGTTGGG GATGTAATTC 2340
ACTCAGGAGG CACTGGCTGC CCTCCCGGCG TGAGCCAGGC CCTGTGAGCA TTGTCTAGGC 2400
AAAGACAACA GTGTATGTAC CCGAGTCCGA CCCAAAGCTG AGCACTGGAT GTGGTAGGTT 2460
TCATCCTTCA AGGTAGAGAT GAGGAAACAG GCTCAAGGGG CAGCCACATG TGGAGACGTA 2520
GACAGGCTGG GCCTCTTCTC CCTGCCCACC TTGTCACCTG TGTCCTTTGA TGATCATACG 2580
CTTGTTCTCC CATGGATTGA CCTGCTCCGA GCATTCTGCC TGGGACCCCA TTTCTGCACC 2640
TCGGAGGCCC CGAGACTTCA TCTCTCCCTC CCCGCGAGAT TCTCCCGCCG CTGAGCTGCG 2700
TTGGCGGCTT GGGGTGTGTG GGCTGATGCT CTTGTGGAGC AGAGCTGTTG CTGGGCAACT 2760
GCTCTGGTGG GGCGGGGGAC GGTGTCGCTC CCAACTTCCT TCTGTCAAGG TGTGGGCTGA 2820
GGCCAGGGCC CAGGTGGGAG AAGAAGCCAG GCAGGGTGTG AGAGACCTGG GCCAGGGATC 2880
TGGTGGCCAG AAGGGAACTG GGATGGAAAG AGGAAAACGT GGGCAAAAGT TCAGCAGAAG 2940
AGGCAGGACT GTGAAAGAGG TTGCATTTAG GGTTTCTAGT TGGGTCACAT TGGCATTTTA 3000
GGGGCATCTT GAGAAGAAGG 3020