EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS127-26719 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr6:34190850-34193960 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs114760566chr634192036hg19
TF binding sites/motifs
Number: 13             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXH1MA0479.1chr6:34193674-34193685TGTGGATTGGA-6.62
Gfi1bMA0483.1chr6:34190862-34190873AGCTGTGATTT-6.14
KLF16MA0741.1chr6:34191865-34191876GGGGGCGGGGC-6.02
KLF5MA0599.1chr6:34191808-34191818GCCCCGCCCC+6.02
KLF5MA0599.1chr6:34191281-34191291GGGGCGGGGC-6.02
KLF5MA0599.1chr6:34191866-34191876GGGGCGGGGC-6.02
RREB1MA0073.1chr6:34192052-34192072CCCCCACCCACGCCCTCCCC+6.77
RREB1MA0073.1chr6:34193828-34193848CCCCACCCCACCCCCAGACC+7.34
SP2MA0516.2chr6:34191278-34191295GAAGGGGCGGGGCGAAG-6.18
ZBTB18MA0698.1chr6:34193249-34193262TATCCAGATGTTA+6.21
ZNF263MA0528.1chr6:34191525-34191546CTCCTTTCTCCTCCCTCCCCT-6.01
ZNF263MA0528.1chr6:34191521-34191542CTCCCTCCTTTCTCCTCCCTC-6.52
ZNF740MA0753.2chr6:34192046-34192059ACACCCCCCCCAC+6.82
Number of super-enhancer constituents: 17             
IDCoordinateTissue/cell
SE_15387chr6:34190899-34193011CD4_Memory_Primary_7pool
SE_18188chr6:34190627-34193089CD4p_CD25-_CD45ROp_Memory
SE_19450chr6:34191031-34191947CD4p_CD25-_Il17p_PMAstim_Th17
SE_19450chr6:34191975-34192963CD4p_CD25-_Il17p_PMAstim_Th17
SE_26784chr6:34190782-34192566Esophagus
SE_26784chr6:34193152-34197543Esophagus
SE_32269chr6:34191136-34192580Gastric
SE_32924chr6:34190866-34191738H1
SE_32924chr6:34191898-34192442H1
SE_34365chr6:34190859-34192745HCT-116
SE_34365chr6:34193286-34198815HCT-116
SE_38509chr6:34190839-34193085HUVEC
SE_40020chr6:34190944-34192835K562
SE_57546chr6:34192000-34192434VACO_503
SE_63029chr6:34190859-34207435Tonsil
SE_65500chr6:34190860-34193304Pancreatic_islets
SE_68752chr6:34190784-34192504H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr63419172634192136
chr63419090334191051
chr63419314434193230
chr63419240034192927
Number: 1             
IDChromosomeStartEnd
GH06I034223chr63419086334193565
Enhancer Sequence
GATGATGGTA AGAGCTGTGA TTTATTGAGC ACTTAATGGA TGCTAAGTCC TGTGCTGCCT 60
CACTTAGTGC TCACCCTGCT GTATAGCAAA CAGGGCCCAG GCAGGAAATG GAATCCAACC 120
AAAGGGTGCA AGAGGCTTTA ATGGAAGGAC GACAGGGGTG GGGGCAGGGT GAAGGGGATC 180
AACCTGGGTA TTGGGACCGG CAGTGATGAC AAGACACTGC AACTTCTGGG CTGAAAGGGC 240
AATGGGAAAA TGCAGTGTTC CCGAGCTGAC ATCATGAGGG GGCATAGCCA CAGTCAGACC 300
AAGGACCAAA ACAGGGCCAG GAGTACCCTG ACTTCTCTCT CGCCTCCCCT CAGGTCGGCT 360
GCATGGGTGC TGCTCAACAG AAAGCCAGCT GGTAAGGGAG CCCGGGCCAC GAAGTCGGCA 420
TGGGAGGGGA AGGGGCGGGG CGAAGGAAGA ATAACAAGCA TAGGGAAGCA GGATTATCCT 480
GCTCCATGCC ATTTCGCAGA TAAGAAGACT GAGGCCCAGA GACATGAAGT AACCTGCCGG 540
CTGCCACAGA GCTGGGAAGG TGGAGCTAGA GGAGAGCCAG GCTCTGAGGC CCTCCGCCCA 600
GCCTCCTAAT ACAATCCCAG CCTCAAGGCG CGAGCAGAGC GCGGAGCAGG CCAGCACCCC 660
ATGCTCCCGG TCTCCCTCCT TTCTCCTCCC TCCCCTCACT GCTCAGCTCT CCCACCCTCC 720
CACCTTCTGT CTGCCTTAGC TGGGCCTCCC CTGGCCTCCT CTCAAGAAGG CTGTGGCCCC 780
TTTCCTCTGT GTGCTTCCCC ACTTTGTCTC TCCCTTTTTT CTCAGTCTTC TTGTCTCCCT 840
CACTCAGTCG CTGTCTTCAT TTCCCTCAGT CTTTCCCTAT AGCAGGCTCA CAAGGGTGCA 900
TCCTCCTAAG GCTCAGTTTC TTTGCCATTC CCGAGCTCCG CCCCCTCTGC CCGCCGTGGC 960
CCCGCCCCTG CCGGGCCGCC CTCCCCTGCG CTGGGCGGCG GGCCGGGTGG CAGGCGGGGG 1020
CGGGGCCCGG GCTGGCGCGG CGCCGGCCTG AGTCACACGC ATGAGGCAGC GTGAGTCAGG 1080
CGCGGAGGGA AGTCCCTGCG GAAGGGGCTT TCGGAGCTGC AGTCGAATCG CAGGGAAAGA 1140
GAAAGTGTTC GAAACGCTGC TTTGACACAG TGACCTTGTG TGAGCCCTAG CTGCACACAC 1200
CCCCCCCACC CACGCCCTCC CCGCAGACAG CAGCACGCAC ACCCCCGGCC GGCTCACGGT 1260
ACGCGGCCGC TGCCCGCACT CCCGGGTCGG GCCTGCGCGT CCCTGTGGGG TTGGGCGAGC 1320
GGGGTATCGA GGGTCCAGCA GCCTGGACCC GGCCCCTCCA CAGGGCAGTC CCTTTTCCAG 1380
CTTCCAAAAG CTAGCGTTGC TCACCTACTG CCAGACCCCA GACCCACTTC TCCCACGAGG 1440
TGTAAAGAAG GACCCCTGAG GGTCTTCCAC GTCACCTTGT GGAGCCTCGT GGAGTATGGC 1500
AGAAGGAGGA GGGCAATTTG AGGTCCTGCA GCGCCCGGGG GAACCAGGGA TGAACTCCCT 1560
CCTGCCCCCA GGCTCTCCTC CTCATCCTAG AATCAATCGA TGGGATTCAG TTACAGAAAT 1620
ATTTATTAAA CACCGACTAT ATGCCAAGTT ATAAAAACCT GGGACAAGAT GGTAAACAAA 1680
GCAGGACAGT AAACAAAATA TATTAACCCC TGCCTTTCAG GAACTGGCAT TCTAGTTAGG 1740
TGAGGGAGAT GATAAACAAA AAATAAGCAA ATGATCTAGG CTAGTGCTGC CCGATAGAAA 1800
TAGAAGGGAA GCCATGAATG TAATGTTTAA TTTTGTAGTA ACCATGTTAA GATGGTAAAA 1860
AGAAACACAT GAAATTAACT TTAATTTTTT TTTTTGAGAC CGAGTTTCGC TCTTGTTGCC 1920
CAGGCTGGAA TACAATGATG TCGACTCACC ACAACCTCTG CCTCCTGAAT TCAAGCAATT 1980
CCCCTGCCTC AGCCTCCCAA GTAGCTGGGA TTACAGGTAT TCACCACCAC TCCTGACTAA 2040
TTTTGTATTT TTGGTAGAGA TGGAGTTTCT CCATGTTGGT CAGGCTGGTC TCGAACTCCC 2100
GACCTCAGGT GATCCGCCCG CCTTGACCTC CCAAAGTGCT GGGATTACAG GCGTGAGCCA 2160
CCGCGCCTGG CCAATTTTAA TTTTTTTTTT TAAGGAACCG GGTCTTCTTA AAGGGTTCCT 2220
TAAGGAACCA GGTCTCTACT TTGTGGTCCA GGCTGGAGTT CAGTGGTGCG ATCATACCTC 2280
ACTGCGGCCT CCAACTCCTG ATGCTCCTGC CTCAGCCTTC CAAAGCCCTG AGATTACAGG 2340
CGTGAGCCAC TGGGCTTGGC CAAAATTAAC TTTAATAATG TATTCTATTT AATCCAATAT 2400
ATCCAGATGT TACCATTTCA ACATGTAATC AATATACAAA AAACTATTGA GTTTTTCTTT 2460
TTCTTTTTTC TTGTACTAAG CCTTGTAAAT CCAGTGAGTA CTTATACTTC CAGCACATTT 2520
CAGCTCAGCC TGAACACATT CCCAGCACTC AGTGGCCACA TGTGCCTAAT GGCTATAGCA 2580
ATGGGCAGCA GAGTCTTGAT GTTAGATGTG GGCTGTGGAA CATAAGGAAA GTAGAGGCGG 2640
GCAAAGGGGC TGGGATAGGA AGCGCTAAGT GGGGGTGGTC TGCCCTGGGC AGCCCTGACC 2700
GGGTGGTGAG GACAGGAGTC GGGCCACAGA TAAGACCTGC AGATTACCTG CAATCTGAAT 2760
CCAGGCTTGG CCACTGGCCT TCGCAATTCA CCTGACCTTG CTGAATAAGG GCATTTTCCT 2820
CCAGTGTGGA TTGGAGTTAT GCATCTGAGG CTATGAGGCA CTCATTAAAT GTTATCCTTA 2880
TCTCACCTGT CTGCAACAGT AGGCAGGGCA CAGGCCCCCA ATCTCAGAGT CACATCCTTT 2940
CCACCCGCAA CTCTTATGGC CACCAAAGGC GGCCTATGCC CCACCCCACC CCCAGACCCT 3000
CCATCTTTTA TCCATTTCTA CTCCTTGCTA CAGCAAGATA CTTAACCTTC TCAGGCTTCT 3060
GTTTCACTAC GTAGTAGGTG CTTTAAGCTC TTCAAAGAAA AGCATTGTAG 3110