EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-14510 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr9:92056250-92058690 
Target genes
Number: 5             
NameEnsembl ID
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:92057415-92057433GCAAGGAGGGGAGGAGGG+6.21
JUN(var.2)MA0489.1chr9:92058018-92058032AGGAGGTGACTCAC+6.17
KLF13MA0657.1chr9:92056823-92056841TGGCCACGCCCATGTTTG+6.52
Klf12MA0742.1chr9:92056824-92056839GGCCACGCCCATGTT+6.64
SP4MA0685.1chr9:92056822-92056839ATGGCCACGCCCATGTT+6.02
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_03177chr9:92056515-92057224Brain_Angular_Gyrus
SE_03905chr9:92054548-92064883Brain_Anterior_Caudate
SE_04779chr9:92053976-92080229Brain_Cingulate_Gyrus
SE_05782chr9:92054240-92082406Brain_Hippocampus_Middle
SE_06723chr9:92053932-92078733Brain_Hippocampus_Middle_150
SE_07735chr9:92054317-92080642Brain_Inferior_Temporal_Lobe
SE_09170chr9:92054083-92061427CD14
SE_11477chr9:92055725-92059917CD20
SE_14475chr9:92054408-92060484CD4_Memory_Primary_7pool
SE_15940chr9:92058193-92060155CD4_Naive_Primary_7pool
SE_16354chr9:92057286-92060391CD4_Naive_Primary_8pool
SE_16924chr9:92057908-92060489CD4p_CD225int_CD127p_Tmem
SE_17355chr9:92053993-92065524CD4p_CD25-_CD45RAp_Naive
SE_17792chr9:92054086-92062874CD4p_CD25-_CD45ROp_Memory
SE_18250chr9:92053940-92065020CD4p_CD25-_Il17-_PMAstim_Th
SE_19118chr9:92054561-92061664CD4p_CD25-_Il17p_PMAstim_Th17
SE_20089chr9:92058324-92061549CD56
SE_21155chr9:92058310-92059883CD8_Memory_7pool
SE_21665chr9:92058225-92060796CD8_Naive_7pool
SE_21969chr9:92054607-92056749CD8_Naive_8pool
SE_21969chr9:92057987-92060891CD8_Naive_8pool
SE_22409chr9:92054663-92057531CD8_primiary
SE_22409chr9:92057540-92062777CD8_primiary
SE_26933chr9:92054283-92059600Esophagus
SE_32149chr9:92054630-92059435Gastric
SE_41833chr9:92054598-92058769LNCaP
SE_50088chr9:92054675-92059690Sigmoid_Colon
SE_52548chr9:92054715-92057464Small_Intestine
SE_52548chr9:92057492-92059510Small_Intestine
SE_53415chr9:92056477-92058276Spleen
SE_60002chr9:92014899-92064443Ly4
SE_62222chr9:92014516-92154755Tonsil
SE_68703chr9:92054492-92059072H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr99205720092058400
chr99205794092058482
chr99205675292056898
Number: 1             
IDChromosomeStartEnd
GH09I089439chr99205461392061272
Enhancer Sequence
ATCAGGGAGG ACTCTTCAGG AATTTGGCAC CAACAACATT AGCTTTCCAG GCAGACAGAA 60
CAGCAGGCAA GACAGAGCCC AATGTGTCTG GGATCAGAAG GAAAGGGGAT GTGGCCGAGG 120
TGATGATGGC AGAGGCAACC CTGAGCTCTG GCTGGAGATG TCGGTACCGG CCAGGCCCCC 180
ATTCCCACAT CATGGGCCAC CCCCACATCA CTGTGTCAGG ATCAGAATGC CCCAGACCAT 240
GGGAAGGAAG TGAGGGCAGC CTGGAAGCAG CAGGCAGGGA GGGGACCAAT TCCCCACCAC 300
CCCATGGCTC CTCCTCAGGG CTCCTGGGAC CTGCCTGGAG GCTGTGGCTG CTTTGTCCCT 360
GGGTGTCCTC AGTACCCTCT TTGTCATTTC AGCCCCAATA CCTGTCTAAC CACTCTGCGT 420
CCAGCTTTCC TGCCTGGGCC CTAACCCCCC TCCCACACTC CCATCCCAGC CCACACTGTT 480
AAACTTCAGC TTCTGATCTA AGTGAAAGGG AAGTCCAGCA ACTCCAGGCC CCACCGTGTG 540
GACAGAGGGC TAGAGGCTGG CAAGAGGGGC TCATGGCCAC GCCCATGTTT GACAGTCCCT 600
CACCAGGCAC CCATCCCCAT GGCTGTGTTT ACACATTTCT CTTCCCCATT GGACTGTAAG 660
GCTCTGTTAT TTAACGTGCC TGAAATCTTG CACAGTTCAT GGATGTGTAG ACCAGCAATG 720
GCCAGGCTGG TGAGTTCAGC ATGTTCCTGA TCACCCCTCC CCATCATCAG CACCCAGTGA 780
GCTGGGGCTG TTTCCTTCCC TTTTCCCCTG GCCCAGGACA CATCTTCAGG CCAGAGACAT 840
GGTTTGCTGC GCCGTACGGC CCAGGTCAAG GTCACTGGCC AAAGCACTGG GAGGGGCTCA 900
GTGGGTCGGC TCTGGGCACC ACGGCTGCCA CGAGGGTGGT AGGGGCTGCT GGAGCCCCCC 960
ACTCCAGCCC CACTGGCCCG CCTGTCAGAA GAGGAGGGAG CTACCTGCTC TTTCCAAGCT 1020
TGCCAGGCTC CAAGAGTCCT CTGTTAAACA TGGCAGCTTT GCAGGAAGAA TACGGACCTC 1080
ATTAGTTAAA ATGCAGTGGA ATAGAAAAAA TTGTAAGAAA ACCATGCAGC AGCAGCAACA 1140
TGTCAAAAGA GTGAGATGGT CAGCAGCAAG GAGGGGAGGA GGGGTGGGCG CCATCTGAAA 1200
CCATGCATAA AAATAAACCA TCTGCCTGGC CGGGGTCCTC TTCCTCTACT TGCTAGAAAC 1260
ACAGAGTTCA AGGTAAAAAT GGAAAAGACA ATGAGTTTCA CTTCCACAGG CCCCAACAGC 1320
TAGCAAAGAA TCAGACCCAC TCACCCTGAG CTGTCAGGAT ACATGCAAGG GGAGGGGAGG 1380
GTTCCTGGGG TTCATAACTG CATCCGTCCC AGAGAGGGAT CAGCACCAGA CAGTGTCTGG 1440
CATGGCTGCA GCCCTCCCCA TCCTTCTCAC CATTTCCCAG CGAGGAAACA CCAGACCCGG 1500
GCAGATGTGA GTCAATGCTG GGGACCCTGG TTCACGCATG TGCCGGTGTC GTCTGCAAAC 1560
CTGGGCCCCG GGCCTGGGCT GGGACAAGCC TGTCATCACA CAGCCTGTGA GACTTTTAAG 1620
GGCCTTCACT GGGGCTAGAG CAACCTCGGA TGCCCACCAG GACCGTGCTC AGCAGCAGGA 1680
GGGCCCCCTG CACCCCTACA GCATGCCTGC ACAGCCTCTG CCTGACCTGG GACTGAAGCC 1740
TCCCAGGAGG AAGGCGGCTC TTCTCCCCAG GAGGTGACTC ACAGTCCAGA GCCCAGCCCC 1800
ATCAGGTCCC CTAGGGACTT CTCCACAGCT TCAAGAGTGA GACTTCCCTG TCAGTGGCGG 1860
GATTATGACC ACCCACACTA CCCCCCTGGA CAGAGGCCGG GTCGCGAGGT GCTCTGGAGA 1920
AGAACGGATG CCAGTGCTCA ACTGGACACA CACTCCAGCC ACAAGCCATA TGTGGGCTGA 1980
ACAAGGAGCT TAAACAGGGC CACCAGGATG CCCATGGGCC CAGTCTCCAG CCACCTTCCC 2040
ACGGGGCCTG GCTGCCCTGT CCACCTTCTC ACTGACCTCG AAGCGGGTGT ACCACGGTCC 2100
TGTTGTCCCT GCAGAGTGGA GCCTTCAGCT GTCTGACAGA AAATGAGCCC TCCCAGTAAA 2160
GCACAGCGTG GACTCCACCC GCCCATAATA GCCACCCGGG AAGCAGGTCC GGCCAGCAGC 2220
AGCCGCCAGA GGAGGATCTG CCTGGGGTAG GCGGGTGGCG GACGGCCCTG GCCCTGCAGC 2280
GCTCAGCTGC ACCCCACCCC ATGCCTGCCT CCGAGCTGGT GGCCAGGACC TGGCTGCCTC 2340
CTGTCCTGGC TGTGAGTCCT GTATGGGCTG GCACCTGAAA CTCTCTACCC TCCCTCCACA 2400
GCATGGGTGG GGCTGGGGTC ACCAGTGGGT AACTGCAGGC 2440