EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS127-04632 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr10:106083780-106086090 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR1MA0112.3chr10:106084910-106084927GAGGTCACAGTGAGCTG+6.48
EWSR1-FLI1MA0149.1chr10:106084159-106084177GAAAGGAAGTGAGGAAAG+6.35
ZNF263MA0528.1chr10:106086045-106086066CCTTCCTGTTCCCGCTCCTCC-7.21
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00742chr10:106084541-106101069Adipose_Nuclei
SE_01164chr10:106083324-106084650Adrenal_Gland
SE_01164chr10:106084653-106086494Adrenal_Gland
SE_04416chr10:106085041-106086395Brain_Anterior_Caudate
SE_06314chr10:106082996-106084450Brain_Hippocampus_Middle
SE_06314chr10:106084659-106100825Brain_Hippocampus_Middle
SE_09405chr10:106080342-106094322CD14
SE_15073chr10:106081435-106084837CD4_Memory_Primary_7pool
SE_15073chr10:106085566-106087017CD4_Memory_Primary_7pool
SE_16277chr10:106083837-106084575CD4_Naive_Primary_7pool
SE_17744chr10:106080942-106099533CD4p_CD25-_CD45RAp_Naive
SE_18973chr10:106081229-106084752CD4p_CD25-_Il17-_PMAstim_Th
SE_18973chr10:106084830-106099514CD4p_CD25-_Il17-_PMAstim_Th
SE_20297chr10:106081116-106091682CD56
SE_22733chr10:106081333-106084480CD8_primiary
SE_22733chr10:106084833-106091284CD8_primiary
SE_26115chr10:106084740-106092852Duodenum_Smooth_Muscle
SE_26588chr10:106075967-106086666Esophagus
SE_29918chr10:106084837-106086120Fetal_Muscle
SE_31767chr10:106084803-106086501Gastric
SE_35928chr10:106080462-106084271HMEC
SE_38084chr10:106083444-106094070HUVEC
SE_40625chr10:106080428-106100998Left_Ventricle
SE_42144chr10:106080334-106100956Lung
SE_45613chr10:106075586-106084478Osteoblasts
SE_45613chr10:106084743-106100882Osteoblasts
SE_47282chr10:106085731-106101028Panc1
SE_48584chr10:106080512-106084745Right_Atrium
SE_48584chr10:106084793-106100937Right_Atrium
SE_49548chr10:106085414-106086449Right_Ventricle
SE_50763chr10:106084795-106092025Sigmoid_Colon
SE_53237chr10:106084961-106086676Small_Intestine
SE_53434chr10:106080815-106094302Spleen
SE_55990chr10:106085780-106092333u87
SE_63125chr10:106067855-106110489Tonsil
SE_67964chr10:106085780-106092333u87
SE_68888chr10:106083122-106084830H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr10106084200106084414
chr10106084006106084523
chr10106085298106085504
Enhancer Sequence
TGTAAGTAGG AGTTGACTTA TTGCACATTG GGAGGAGGTG GCTGGTGGCA GATAGAGCTG 60
GGGAGTGACA TGTCTCCACC AACTCCCTCC TTGTTGCCTA ACTCAGGACA GAGGACACAG 120
CACAAATGGC TCAGTAACAA TGGCTCTGAA TGTGTCACTG CTCAGCCTGA TTGGCTCCCA 180
TCCTTCCAGG ACAGTGGGAC AGGAGAAGGG CTTTGCTCCA GCAAGTGCAA GGTCTCAGAG 240
CTGCTCCCAC CAGGGCATCT CTGGCTGGGT CCCTCTTCAC TTGCACTCCA AATGGGGACA 300
GGAGAGGGAA TATAGAGGGG CAGGTGAGCA GACTGGGGCC GGAGGCTGGG CCCTGAAAGG 360
GGAGGGAGGG ACAGGCAAAG AAAGGAAGTG AGGAAAGAGG AAGGAAGAGG ACCAACAAAA 420
AGATCATTGA GAAAGTAGGT GGAAAGGGTG CGTTTGCGGC TCTGGGCTTG CCGCACTTCC 480
TTTTCTTCTC GGCGTCCTTG CAGCCCTGAC CCCGTCCAGT CATCTGCCCC CTCTCCCACT 540
GGGCAGGACC ATCATGTTGG CCAACCCACC TCCCCCAGAC CTGCCACCCT GTGGCCACTG 600
GGCTCCTTCC CTTCCTCTCT CCAGACACCT GTCTCGAGGA CCCGGGTTGT AAAATCAAGT 660
GTCTGGGAGG GCCAGCCCGC AGGGAAAATG AGCGGGGCTG CAGTGGACAG CTGAGAGGAG 720
GGGACACTGG TCGACTGGAT GGCACATGCT TCGTCTGAAG GGGCGAGTCC CCACGCCACA 780
CATTCTGTGC ACCCAGAATG ACAAGATCTT TTTTTTCCCA AAGAAAAGCC ACTAATCTGG 840
ACTTTGTCAA AATCCCCCCA TTTTTAAATG TTAGCTGCTA TTTCAAAAAT TCCTTAAAAA 900
CCATGTGAGC AACACTGGGT GCAGTGGCTC ACACCTATAA TTCCCAGCAC TTTGGAAGGC 960
TGAGGCAGAT GGATCGCCTG AGCTCAGGAG TTCGAGACCA GCCTTGGCAA CATGGCGAAG 1020
CCCCGTCTCT ACCAAAAATA TAAAAAAACT AGCTGGGCGT GGTGGCACAT GCCTGTGGTC 1080
CCAGCTACTC AGGAGGCTTA GGTGTGAGGA TTGCTTGAGC CCGGGAGGCG GAGGTCACAG 1140
TGAGCTGAAA TGGCGCCACT GCACTCCAAC TTGGGTGATA CAGTGAGACC TCGTCTTGAA 1200
AAGAAAAGAA AATGAAATAA AATATGTTAG TGGCCACCCA GAGCCTGTGG GCTCTGGTCT 1260
GCAACCCCCC ATGAAGCGTT CCTCAAGGTA ACCCCTAACC CAGGACTCTC CTTACTCCTA 1320
CCCCATCAGC AACTACTCAG CAAACCCACT ATTTCCTCTG AGTCCATGAC TCCCTGAAAT 1380
ACTGGCTCCA CCTTTCTCCC CAAACCTAGG CCTGATTACT CCCGTGTCTC CTCGTTGGCC 1440
CCAGCAGCCA CATTCGGAAT AATCCTAACC AGCACTTATG AGGGCTGACT CTGTGCCAGC 1500
CCTTGTAGGA ACTTAGTGTA AATGCCAGAG CAGATTTTCT TCCTTCCCCA TGGCCTCTGC 1560
AAGGACTAGA AGAAAAGAGA GAAGAGGCTT TGTTGGGTTG GCATCCTGGT GACTTTTTTT 1620
AAGTCCCTCC CTCTTCCTAG AATGGGCCTT GAGGACACTT AATGCTTCGA GTGGGTGGAA 1680
CCGGGCACCC CGAGTCCAGC CAGCGTGTGC ACACGCGGAC AGCAGAGGCT CGCCTAAGCA 1740
AAAAGGCCTA ATGGTGCTGC GCTAAGAAGC GCTTGGTATT AGAGTAAGGC CTGTGGGCCC 1800
CAGGAGCCCC AACTGTCCCT CCCTAACCCA GGGGAGAGCC CAGACTGACT GAGTGGGATG 1860
CTGGGCTCAG AAGCACCCAG GGGTCAGTCT GGACTCTGGT GAGGTGGGGC AGCAGGACAG 1920
ACAGCAGAGA GGGGAGAGCT CCACCCCAGT GCCCACCTGA GGTGGCCCTA CCACCGAGCC 1980
GGTGGGGAAG TACACGCGGG GCAGAAGCTG CCTTTTTTTG CTCCAGCGAG CCTCTGTTGT 2040
CTGCATGTGG ACACTCTGGC CGGACTCACA GGAGGTGCTG CTCACACCCG TCCAAAGCAT 2100
TAAGTGCTCT CAAGGCCCAC TCTCGGGAGA GGGAGCGGTT TCAAGAAGTC ACCAGAATGC 2160
CAACTCTGTT CTCAGGACTG GGTCATGGGG GTGGTCTGCC AGCCAGCAGA GGCACAGGAA 2220
GGACAGAGGG CTGGACTCTG CTGGCTCTGG GTGGGTGAGC CACATCCTTC CTGTTCCCGC 2280
TCCTCCGCCG GCTGATGCAC GTCCCTCGGC 2310