EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-07467 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr19:18228160-18230830 
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
GAGACTGAGG CTGGAGTTCA ATCAGGTGGC TGCTTCCTAA CTGAGGCAGG GCTGATGGCC 60
TTTCCCGCCA CACACAGACA GAGCATGTCA GACGCCCCGA CTCAATTTGC CAAACACACC 120
CTCTATGCCA GTCCGGTGCT GGGAGCTGCT GGGACCCTAA GGAGCCCCCA GCCTGGGGAA 180
GACATAGCCG GACAGACAGG AAAGCGGGTT TTTCAGAGGA GAGGACGCAG TTTTGCCAGG 240
CTAGATTCCA AGCAGTGGGG CCAGGGTGGG CGTGGTAGCA TGAGCCGGCC AGGACGCTGG 300
GGTGGGTCTT GGGTGCCGCA CTGAGAAGGG GTCAGTGCTC TGGGAGAGAG GAAAAAGATG 360
GAGGGAGCGA TTAGATTTAC ATTTTAGCAG AAAGGAGCCA AAATGCCTGC CCCTAGCTCG 420
AGGTTAAGGT GCTGCCAACG CCCCGCCCCC GCCGCCCGCG GTCGTAGCAA CGCCCGGCCT 480
CAGCCGCCCG CGGCCCTAGC AACGCTCCGC CTCTCCGCCC GCGGCCATGG CAGCGCCCCG 540
CCCACTCGCC GGCACGCGGG TCCGCCGGCC TCGCTTCCGC GTCGCTCGCT CCGCCTCCCG 600
ACAGGCCCCG CCCCCAACGG CCCCGCCCCC GCACTCGCCT GGGCGGAGTT CCAGTCGCGC 660
TCGGGGGCGC GCGCTTCCTT CTCGCCGCCC CCCCATCCCC GCAGCCCCGT GCGCCCCCCT 720
CCCTGTCCGG CTCCGCGGGG CTCCTGGGGC CGATCCCACC GCCGAGGCCT CCCTTCCCGG 780
CCTCGGGCGG CTGCGGCGGC ACAAAGGGAA GCAGCATGTC CGACCCCAGC TACTGGACGG 840
CGGTGGCGGC TCCCGGCCAT CGGAGCCGCC TGGCAAAAGG CGCGCTGCTG CAGCGCTCCA 900
AGAGGTAGGG GGCACGGCGC CGGCGAAGGC TCGGCGGCCA GCCGAGCAAA CAGGAGTTGC 960
CAGAAGTGTG TCCTGGCCGC GTGGCGCGGA CCACGGCGAG CGTCTGTCTG TGGCAGCAGT 1020
GGGAAGGGGG GAGGACGCCT GTGGATCGAG GTGTCCCCTG GGGTCCCTGG CACCCTCCTT 1080
TCGCCCCTCG TTCCCTGGAC TGGGGTGTCT GTCCGCCAGC GTCGCAGCTG GGGTGGTGAC 1140
AGACAGGAGT GAGTTGAGAT TGAGCTAGGA TTTGAACCCG GGTGTCCAGG GCTGGGCAGA 1200
ACCAGGGAGG AACTTCTTGG AAAAACTGAG GCTGATCTGC CGCTGGGGGT CCATTCAGCA 1260
GAAATGTTGG CTCAGAAGCA AATATTTACT GCACGAGGCT GGCATTTGGG TGGGGTGTCA 1320
GGAGTCCAGA TAGTTGGGGT TAACCCCCGC CAAAGCCTCA CCGCTCTTGG AGTCTCAGTT 1380
TCCCCTTTTG AAAAGCAGAG AGGATAAGTG AGGGCTGTGG ATTCTACCAG ACCTGGGTTC 1440
AAATTTCGAC TCAGCCACTA CCAGGCTGTG TGACCTCAAG TAGCTCCTTA ACCTCTCTGT 1500
GCTTGGGTTT CTCATTGGTG CTGGACTGGG GCAAAGTCTG GGCGGTGGGA CCAGCTACCG 1560
AAAGACCTTG AATGCTGAGT CCAGGGCTTA AACTTACCTC CAAGATCGTG GGGAGCATTG 1620
GAGGGGGAAT ATGGGTGCCA GAGGGATGAG GTGCAGGAGG CTGGCTTCAG GCCCCTGCTT 1680
TCTGCCACAT TCTCTCTGTT GTGTCCTGGG TACCAAGAGA GGATCGTTCT CAAATGGCAA 1740
CTTCTCGAGG TCCTGGATCT CCTCCAGGAA GAGTTGAACA AACAGTCGGC CCTGCATAGA 1800
TGCTTGGGAA GTGAACAGAT GATGCTTAGT TCTCCTTTGA GGCCTCACAT TTGGCCGTGT 1860
TTTCAAGAAG ACCTCGCCCA AGAACAGGAG GGAGGGCAAC GAAGTGTTTT TCCCAAATGC 1920
TTTTGGAAGC AGCAAGTGAT ACAGCAGGAT CGGGGAGGGA GGGTGCTGGT GGTGCAGTGT 1980
GGGGGCGAGG AACCAGGTGA GGGGCTGGGA GAGGATGTGG AGACAGCCAG GTGAGCGTGC 2040
ATTGAGGGGT TGGCAGGAAG TTTTGCAGAA ACCTGTGGGT TTCACTTTTG CTTCTGCAGC 2100
TCAGGCTGGG AGACAATCAC TGTGACTGTT GACATCTGTG GCTTCAGTTT CCCAGTCTGG 2160
AAAATGGGCT CAGCTGGTCA TTCCCAACTC TGGGGCTTGT TGGAATTGGC AGATGTTGGG 2220
GATGTAATTC ACTCAGGAGG CACTGGCTGC CCTCCCGGCG TGAGCCAGGC CCTGTGAGCA 2280
TTGTCTAGGC AAAGACAACA GTGTATGTAC CCGAGTCCGA CCCAAAGCTG AGCACTGGAT 2340
GTGGTAGGTT TCATCCTTCA AGGTAGAGAT GAGGAAACAG GCTCAAGGGG CAGCCACATG 2400
TGGAGACGTA GACAGGCTGG GCCTCTTCTC CCTGCCCACC TTGTCACCTG TGTCCTTTGA 2460
TGATCATACG CTTGTTCTCC CATGGATTGA CCTGCTCCGA GCATTCTGCC TGGGACCCCA 2520
TTTCTGCACC TCGGAGGCCC CGAGACTTCA TCTCTCCCTC CCCGCGAGAT TCTCCCGCCG 2580
CTGAGCTGCG TTGGCGGCTT GGGGTGTGTG GGCTGATGCT CTTGTGGAGC AGAGCTGTTG 2640
CTGGGCAACT GCTCTGGTGG GGCGGGGGAC 2670