EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS038-10172 
Organism
Homo sapiens 
Tissue/cell
ESC_neuron 
Coordinate
chr19:18228060-18231050 
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
AGATATGGAA CATATACCAG GTGCCCTTGG AAGCGCCCCC TTACATCTGA TTTGTGTAAT 60
TCTCATGTCA GTTCAGTTTT CCTCCAATTT CACAGTTGAG GAGACTGAGG CTGGAGTTCA 120
ATCAGGTGGC TGCTTCCTAA CTGAGGCAGG GCTGATGGCC TTTCCCGCCA CACACAGACA 180
GAGCATGTCA GACGCCCCGA CTCAATTTGC CAAACACACC CTCTATGCCA GTCCGGTGCT 240
GGGAGCTGCT GGGACCCTAA GGAGCCCCCA GCCTGGGGAA GACATAGCCG GACAGACAGG 300
AAAGCGGGTT TTTCAGAGGA GAGGACGCAG TTTTGCCAGG CTAGATTCCA AGCAGTGGGG 360
CCAGGGTGGG CGTGGTAGCA TGAGCCGGCC AGGACGCTGG GGTGGGTCTT GGGTGCCGCA 420
CTGAGAAGGG GTCAGTGCTC TGGGAGAGAG GAAAAAGATG GAGGGAGCGA TTAGATTTAC 480
ATTTTAGCAG AAAGGAGCCA AAATGCCTGC CCCTAGCTCG AGGTTAAGGT GCTGCCAACG 540
CCCCGCCCCC GCCGCCCGCG GTCGTAGCAA CGCCCGGCCT CAGCCGCCCG CGGCCCTAGC 600
AACGCTCCGC CTCTCCGCCC GCGGCCATGG CAGCGCCCCG CCCACTCGCC GGCACGCGGG 660
TCCGCCGGCC TCGCTTCCGC GTCGCTCGCT CCGCCTCCCG ACAGGCCCCG CCCCCAACGG 720
CCCCGCCCCC GCACTCGCCT GGGCGGAGTT CCAGTCGCGC TCGGGGGCGC GCGCTTCCTT 780
CTCGCCGCCC CCCCATCCCC GCAGCCCCGT GCGCCCCCCT CCCTGTCCGG CTCCGCGGGG 840
CTCCTGGGGC CGATCCCACC GCCGAGGCCT CCCTTCCCGG CCTCGGGCGG CTGCGGCGGC 900
ACAAAGGGAA GCAGCATGTC CGACCCCAGC TACTGGACGG CGGTGGCGGC TCCCGGCCAT 960
CGGAGCCGCC TGGCAAAAGG CGCGCTGCTG CAGCGCTCCA AGAGGTAGGG GGCACGGCGC 1020
CGGCGAAGGC TCGGCGGCCA GCCGAGCAAA CAGGAGTTGC CAGAAGTGTG TCCTGGCCGC 1080
GTGGCGCGGA CCACGGCGAG CGTCTGTCTG TGGCAGCAGT GGGAAGGGGG GAGGACGCCT 1140
GTGGATCGAG GTGTCCCCTG GGGTCCCTGG CACCCTCCTT TCGCCCCTCG TTCCCTGGAC 1200
TGGGGTGTCT GTCCGCCAGC GTCGCAGCTG GGGTGGTGAC AGACAGGAGT GAGTTGAGAT 1260
TGAGCTAGGA TTTGAACCCG GGTGTCCAGG GCTGGGCAGA ACCAGGGAGG AACTTCTTGG 1320
AAAAACTGAG GCTGATCTGC CGCTGGGGGT CCATTCAGCA GAAATGTTGG CTCAGAAGCA 1380
AATATTTACT GCACGAGGCT GGCATTTGGG TGGGGTGTCA GGAGTCCAGA TAGTTGGGGT 1440
TAACCCCCGC CAAAGCCTCA CCGCTCTTGG AGTCTCAGTT TCCCCTTTTG AAAAGCAGAG 1500
AGGATAAGTG AGGGCTGTGG ATTCTACCAG ACCTGGGTTC AAATTTCGAC TCAGCCACTA 1560
CCAGGCTGTG TGACCTCAAG TAGCTCCTTA ACCTCTCTGT GCTTGGGTTT CTCATTGGTG 1620
CTGGACTGGG GCAAAGTCTG GGCGGTGGGA CCAGCTACCG AAAGACCTTG AATGCTGAGT 1680
CCAGGGCTTA AACTTACCTC CAAGATCGTG GGGAGCATTG GAGGGGGAAT ATGGGTGCCA 1740
GAGGGATGAG GTGCAGGAGG CTGGCTTCAG GCCCCTGCTT TCTGCCACAT TCTCTCTGTT 1800
GTGTCCTGGG TACCAAGAGA GGATCGTTCT CAAATGGCAA CTTCTCGAGG TCCTGGATCT 1860
CCTCCAGGAA GAGTTGAACA AACAGTCGGC CCTGCATAGA TGCTTGGGAA GTGAACAGAT 1920
GATGCTTAGT TCTCCTTTGA GGCCTCACAT TTGGCCGTGT TTTCAAGAAG ACCTCGCCCA 1980
AGAACAGGAG GGAGGGCAAC GAAGTGTTTT TCCCAAATGC TTTTGGAAGC AGCAAGTGAT 2040
ACAGCAGGAT CGGGGAGGGA GGGTGCTGGT GGTGCAGTGT GGGGGCGAGG AACCAGGTGA 2100
GGGGCTGGGA GAGGATGTGG AGACAGCCAG GTGAGCGTGC ATTGAGGGGT TGGCAGGAAG 2160
TTTTGCAGAA ACCTGTGGGT TTCACTTTTG CTTCTGCAGC TCAGGCTGGG AGACAATCAC 2220
TGTGACTGTT GACATCTGTG GCTTCAGTTT CCCAGTCTGG AAAATGGGCT CAGCTGGTCA 2280
TTCCCAACTC TGGGGCTTGT TGGAATTGGC AGATGTTGGG GATGTAATTC ACTCAGGAGG 2340
CACTGGCTGC CCTCCCGGCG TGAGCCAGGC CCTGTGAGCA TTGTCTAGGC AAAGACAACA 2400
GTGTATGTAC CCGAGTCCGA CCCAAAGCTG AGCACTGGAT GTGGTAGGTT TCATCCTTCA 2460
AGGTAGAGAT GAGGAAACAG GCTCAAGGGG CAGCCACATG TGGAGACGTA GACAGGCTGG 2520
GCCTCTTCTC CCTGCCCACC TTGTCACCTG TGTCCTTTGA TGATCATACG CTTGTTCTCC 2580
CATGGATTGA CCTGCTCCGA GCATTCTGCC TGGGACCCCA TTTCTGCACC TCGGAGGCCC 2640
CGAGACTTCA TCTCTCCCTC CCCGCGAGAT TCTCCCGCCG CTGAGCTGCG TTGGCGGCTT 2700
GGGGTGTGTG GGCTGATGCT CTTGTGGAGC AGAGCTGTTG CTGGGCAACT GCTCTGGTGG 2760
GGCGGGGGAC GGTGTCGCTC CCAACTTCCT TCTGTCAAGG TGTGGGCTGA GGCCAGGGCC 2820
CAGGTGGGAG AAGAAGCCAG GCAGGGTGTG AGAGACCTGG GCCAGGGATC TGGTGGCCAG 2880
AAGGGAACTG GGATGGAAAG AGGAAAACGT GGGCAAAAGT TCAGCAGAAG AGGCAGGACT 2940
GTGAAAGAGG TTGCATTTAG GGTTTCTAGT TGGGTCACAT TGGCATTTTA 2990