EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-39497 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr19:18228110-18230310 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10401175chr1918230274hg19
TF binding sites/motifs
Number: 16             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EGR1MA0162.3chr19:18228781-18228795CCCGCCCCCGCACT+6.21
EGR3MA0732.1chr19:18228780-18228795CCCCGCCCCCGCACT+6.83
EGR4MA0733.1chr19:18228780-18228796CCCCGCCCCCGCACTC+6.16
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
TTTGTGTAAT TCTCATGTCA GTTCAGTTTT CCTCCAATTT CACAGTTGAG GAGACTGAGG 60
CTGGAGTTCA ATCAGGTGGC TGCTTCCTAA CTGAGGCAGG GCTGATGGCC TTTCCCGCCA 120
CACACAGACA GAGCATGTCA GACGCCCCGA CTCAATTTGC CAAACACACC CTCTATGCCA 180
GTCCGGTGCT GGGAGCTGCT GGGACCCTAA GGAGCCCCCA GCCTGGGGAA GACATAGCCG 240
GACAGACAGG AAAGCGGGTT TTTCAGAGGA GAGGACGCAG TTTTGCCAGG CTAGATTCCA 300
AGCAGTGGGG CCAGGGTGGG CGTGGTAGCA TGAGCCGGCC AGGACGCTGG GGTGGGTCTT 360
GGGTGCCGCA CTGAGAAGGG GTCAGTGCTC TGGGAGAGAG GAAAAAGATG GAGGGAGCGA 420
TTAGATTTAC ATTTTAGCAG AAAGGAGCCA AAATGCCTGC CCCTAGCTCG AGGTTAAGGT 480
GCTGCCAACG CCCCGCCCCC GCCGCCCGCG GTCGTAGCAA CGCCCGGCCT CAGCCGCCCG 540
CGGCCCTAGC AACGCTCCGC CTCTCCGCCC GCGGCCATGG CAGCGCCCCG CCCACTCGCC 600
GGCACGCGGG TCCGCCGGCC TCGCTTCCGC GTCGCTCGCT CCGCCTCCCG ACAGGCCCCG 660
CCCCCAACGG CCCCGCCCCC GCACTCGCCT GGGCGGAGTT CCAGTCGCGC TCGGGGGCGC 720
GCGCTTCCTT CTCGCCGCCC CCCCATCCCC GCAGCCCCGT GCGCCCCCCT CCCTGTCCGG 780
CTCCGCGGGG CTCCTGGGGC CGATCCCACC GCCGAGGCCT CCCTTCCCGG CCTCGGGCGG 840
CTGCGGCGGC ACAAAGGGAA GCAGCATGTC CGACCCCAGC TACTGGACGG CGGTGGCGGC 900
TCCCGGCCAT CGGAGCCGCC TGGCAAAAGG CGCGCTGCTG CAGCGCTCCA AGAGGTAGGG 960
GGCACGGCGC CGGCGAAGGC TCGGCGGCCA GCCGAGCAAA CAGGAGTTGC CAGAAGTGTG 1020
TCCTGGCCGC GTGGCGCGGA CCACGGCGAG CGTCTGTCTG TGGCAGCAGT GGGAAGGGGG 1080
GAGGACGCCT GTGGATCGAG GTGTCCCCTG GGGTCCCTGG CACCCTCCTT TCGCCCCTCG 1140
TTCCCTGGAC TGGGGTGTCT GTCCGCCAGC GTCGCAGCTG GGGTGGTGAC AGACAGGAGT 1200
GAGTTGAGAT TGAGCTAGGA TTTGAACCCG GGTGTCCAGG GCTGGGCAGA ACCAGGGAGG 1260
AACTTCTTGG AAAAACTGAG GCTGATCTGC CGCTGGGGGT CCATTCAGCA GAAATGTTGG 1320
CTCAGAAGCA AATATTTACT GCACGAGGCT GGCATTTGGG TGGGGTGTCA GGAGTCCAGA 1380
TAGTTGGGGT TAACCCCCGC CAAAGCCTCA CCGCTCTTGG AGTCTCAGTT TCCCCTTTTG 1440
AAAAGCAGAG AGGATAAGTG AGGGCTGTGG ATTCTACCAG ACCTGGGTTC AAATTTCGAC 1500
TCAGCCACTA CCAGGCTGTG TGACCTCAAG TAGCTCCTTA ACCTCTCTGT GCTTGGGTTT 1560
CTCATTGGTG CTGGACTGGG GCAAAGTCTG GGCGGTGGGA CCAGCTACCG AAAGACCTTG 1620
AATGCTGAGT CCAGGGCTTA AACTTACCTC CAAGATCGTG GGGAGCATTG GAGGGGGAAT 1680
ATGGGTGCCA GAGGGATGAG GTGCAGGAGG CTGGCTTCAG GCCCCTGCTT TCTGCCACAT 1740
TCTCTCTGTT GTGTCCTGGG TACCAAGAGA GGATCGTTCT CAAATGGCAA CTTCTCGAGG 1800
TCCTGGATCT CCTCCAGGAA GAGTTGAACA AACAGTCGGC CCTGCATAGA TGCTTGGGAA 1860
GTGAACAGAT GATGCTTAGT TCTCCTTTGA GGCCTCACAT TTGGCCGTGT TTTCAAGAAG 1920
ACCTCGCCCA AGAACAGGAG GGAGGGCAAC GAAGTGTTTT TCCCAAATGC TTTTGGAAGC 1980
AGCAAGTGAT ACAGCAGGAT CGGGGAGGGA GGGTGCTGGT GGTGCAGTGT GGGGGCGAGG 2040
AACCAGGTGA GGGGCTGGGA GAGGATGTGG AGACAGCCAG GTGAGCGTGC ATTGAGGGGT 2100
TGGCAGGAAG TTTTGCAGAA ACCTGTGGGT TTCACTTTTG CTTCTGCAGC TCAGGCTGGG 2160
AGACAATCAC TGTGACTGTT GACATCTGTG GCTTCAGTTT 2200