EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS017-20831 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr20:47354240-47356990 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6066835chr2047355009hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Myod1MA0499.1chr20:47355227-47355240GGGGACAGCTGCT-7.04
MyogMA0500.1chr20:47355230-47355241GACAGCTGCTG+6.14
SOX10MA0442.2chr20:47355989-47356000TCCTTTGTTTT-6.32
SP2MA0516.2chr20:47354320-47354337ATAAGCCCCTCCCATTC+6.37
Sox3MA0514.1chr20:47355990-47356000CCTTTGTTTT+6.02
Tcf12MA0521.1chr20:47355230-47355241GACAGCTGCTG+6.02
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_01671chr20:47354368-47357034Aorta
SE_03141chr20:47353753-47357193Brain_Angular_Gyrus
SE_03860chr20:47352646-47357274Brain_Anterior_Caudate
SE_04767chr20:47330290-47357597Brain_Cingulate_Gyrus
SE_05768chr20:47330773-47357344Brain_Hippocampus_Middle
SE_06681chr20:47321409-47357433Brain_Hippocampus_Middle_150
SE_07719chr20:47329977-47357562Brain_Inferior_Temporal_Lobe
SE_08847chr20:47354585-47355007Brain_Mid_Frontal_Lobe
SE_09151chr20:47353839-47357374CD14
SE_11697chr20:47353783-47356584CD20
SE_14588chr20:47354199-47356996CD4_Memory_Primary_7pool
SE_16488chr20:47355140-47356190CD4_Naive_Primary_8pool
SE_18054chr20:47354068-47357368CD4p_CD25-_CD45ROp_Memory
SE_18819chr20:47354063-47357233CD4p_CD25-_Il17-_PMAstim_Th
SE_19386chr20:47354052-47357337CD4p_CD25-_Il17p_PMAstim_Th17
SE_20065chr20:47354132-47357341CD56
SE_22493chr20:47354199-47357283CD8_primiary
SE_32607chr20:47354044-47358612GM12878
SE_42516chr20:47353714-47355907Lung
SE_42516chr20:47355916-47357322Lung
SE_50554chr20:47354020-47356510Sigmoid_Colon
SE_53697chr20:47354561-47355631Spleen
SE_65415chr20:47354581-47356039Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr204735451247355881
chr204735599447356352
Number: 1             
IDChromosomeStartEnd
GH20I048738chr204735407447357229
Enhancer Sequence
ACTCGAGCTG GAATCACTGG GAAGAGAAAC TCTCTTTGAG CTGCTGTTGA ACCCCTGCCA 60
CCATGTGAGG CATGCACCCC ATAAGCCCCT CCCATTCTCC AAGAGTGAAA TCAGCACTGC 120
ACAGATAAAA GCAGAGCCTG AGATCAGAGA AAGACCTGGT CCTGAAATCA TCATACGGAG 180
TCCTGGATCT AGCTATGCCT GAAGCCAACC TACACTCCTG AACAATTTCA CTGACATGCA 240
TCAGTAAAGT CCTGTATTTG TTTAAGCCTA TCTGAACTGG TGTTTCTGTC ACGTACAGCA 300
AAGACAGTTT TGATACATGC ACACTCTTAA AGGCAGAAAA TGAAAGACAT GGACCCAAAT 360
CTTAGTGAGG TGACAGGGTC TCTCTGTCCA TCTCCACAGA GATGAAGGGA AGGGACTGGG 420
CCAGAAAGCA GGGACAAATC GGTTTCTTCC CACATACCAA CCCCAGTCAC TGGGTAGTGC 480
CAGCTGGAAC ACTGGTGAGG AGGATTCTGG GGCCCCACAG GAAGCCTAGA GACAGAATGC 540
TGTGATTGAT TAGGAATGTC TGCCACAGGT GCAGGAGAGG GGGTAACAAG CTCACCACTG 600
GTTTGTCATT CCTCATCCCC TGAGCCCCCT TCTACGACAA GGTCTGCAAT GTTTTCCTCT 660
CCTTCAGCCT GTGGGAAGGG CAGGGGCCCA ACGCTTGAGG CTTGGAGAAG TTAAATTTAG 720
CAAAGGACAA CATCCCCTCT GCAGCACCGT GCCCAGTTCA ATCACGCCTG TGTCCTTTCA 780
TCCAGCCTGA CCCCAGCTGC ATCTCAGGCC TGAGACCCTG CAAATACGGA AACGCTGCTC 840
TTGACAGCTC AGAGTCCAAG TGTTCCATTT CCTCCTGGAG GCCCGACATG GGGCTCTGAT 900
TGCTTTGCCA GGAAGAAACG GACAAACAGT TGTGCATACA CAGATGTGGT GGGTACGGAA 960
CATGTGGCTG TGGGTTTGGG GGGAGAAGGG GACAGCTGCT GGCTGGAAAC AGCCAGGGGA 1020
GGGGAGCTCA CCCCCAGGAA AGGCTCAAGG ATTGTGAGAG GTGGCAGCTG CTGTCCACAA 1080
TACCCAGGTG ACAGTGGCTC CACAGAGACC ATCAGCTCCA AACCACTCAT TTCACAGCCA 1140
GCAAGACTAA GACCCAGAAG AGGGAAGGAG CTGGCCCATG CAGACATATT CTCCAGTGGG 1200
GAGGAGAGAA GTGAGAATCA GGTCTCAGTT TCTCAACAGT CTCCCCAAAT TATTTACCCA 1260
TCCATACAGC TGTGGGGAGA GGGGGGTTAA AACAGAAATC AGACCACACT ACTCCCGTGC 1320
TTAAAACCTG CAATGGCTTT CACTGACTCA GAATAAGATC TACAGTCCTC ACCTCGGCAC 1380
GCAAAGCCCT ACAGGATCTG CCCTGCCCCC ACTATGACAC CCTCAAACTC TCTCTATCAC 1440
TCACTCTGCT CTGGCCACGC CAGTCTCCCT TCTTCTCTCA AATGAGCTAA GCTTGCTCCC 1500
AGCTCAGGGC TTCTGCCCTT TCTCACCTTG GTCCAGACCA CCCTCCCCAA GATCATCCCA 1560
TTCCAACCCC TCAGAAAGGC CATCCCACCC TTGGGTTGCC AGATATAAAA TAAACCCCAG 1620
GATGCCCAGG TGAATGCTCA TTTCAGACAC ATATTTTTTT TAGTATAAGT ATGTCTCAAA 1680
TATTCCATAA GACATGTTTC CACTAAAAAA TTATTTGATG TTTACCTGAA ATTCCAATTT 1740
CCCTGGGTGT CCTTTGTTTT CATTTGCTAA ATCTAGCAGC CCTGGCCCTG ACCTCCCGAT 1800
TGAAAGCAAC CTCAGGCAGA GTCACTCTTT ACCACATCTG CATTTTATGT TCTTCACAGT 1860
CTGCACTGGC ATCTGAAATG ACCTCATTTG TTAAATTACC CTCTGTTTCT CCCACCTACG 1920
AGCCGCGTGG CAGCACGGAG CAAGTCTGTC TTACTTAGTA CAGCATCCCC AGGGTCTAGT 1980
GCAGAGCCTG GCACACAGGA GATGCTTACT ATGTATTTCA GGAGACCTCA TCACATAAGA 2040
GTAAAAAACA CAGACTCTAC AGCCTGACTG TGTCAGCTCA AATCCTGGCT CTGATGCTTC 2100
CTAGCTCTGT AAGCTTGCCC TATAACTTAA TCTCTCTGGG CCTTGGTTTC CTCATCTGTA 2160
AAATGGGTAC AATAATAGTA ACCACCTTTA AAGAGTGTTG TGAAGTTTTA ATGAATGCAT 2220
ATCTGTAAGG CACAGAGAAC AGAACCCAGC ACAAAGAAAA TGTCCACTCG GTGCTAGTTT 2280
ATGATAAACT CAGTAGTTAG TGGTTGGGTT TTGGGGAAAG GGGGTGAGGG ACTCTTCCCC 2340
CATCTGATCA GTTAGGTGAC ACTAGCGGGC TGGACTGTGG GCCAGGGCCC CTTCCTCTCC 2400
TGGAGAGCCT GTCTGCAAGA GCTCTGTTCC CGATTAGCAT CTCACCAGCC CAGATGCTGC 2460
CATGGCCATG GGAAAATGTT TCCAAGCAGG GAGTAAATGG AGTAAACAAG CCTGGGAAGG 2520
AGAGTGGACC CAGCACCTCT TTCCTTTGGG GCTGCAGTGG ATGCCATGGT GCACTCCTCA 2580
AATGCCTGTC ACAGAGACAG AGACACCCCT TACCCCAGGT GCTGGGAGTG CTGGCTGACA 2640
ATGACCCTCA GCTAAGGCCC TCTCCTAGAG CTGCCTTCAG CCTAAGAGGG CCACCTGTCT 2700
GAGGCGGTAC ACCCACTCCT GAGGACAGCC CACTGGGCAA CAAGGGTGCA 2750