EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS139-56989 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr9:123629240-123631080 
Target genes
Number: 7             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10985068chr9123629724hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr9:123630294-123630305GCCCCGCCCCC+6.02
KLF5MA0599.1chr9:123630294-123630304GCCCCGCCCC+6.02
MEF2CMA0497.1chr9:123630353-123630368TTCTATTTTTGGAGA-6.04
PLAG1MA0163.1chr9:123630945-123630959CCCCCTCGGGCCCC-6.65
SP3MA0746.2chr9:123630293-123630306TGCCCCGCCCCCC+6.01
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_11823chr9:123630403-123631214CD3
SE_13925chr9:123630290-123631203CD34_Primary_RO01536
SE_15579chr9:123630324-123632151CD4_Memory_Primary_8pool
SE_16326chr9:123630227-123632358CD4_Naive_Primary_8pool
SE_16854chr9:123630351-123631205CD4p_CD225int_CD127p_Tmem
SE_17311chr9:123629326-123633344CD4p_CD25-_CD45RAp_Naive
SE_17766chr9:123629615-123633170CD4p_CD25-_CD45ROp_Memory
SE_19108chr9:123630361-123632185CD4p_CD25-_Il17p_PMAstim_Th17
SE_20050chr9:123630318-123632258CD56
SE_20898chr9:123629968-123631224CD8_Memory_7pool
SE_21944chr9:123630159-123632244CD8_Naive_8pool
SE_22312chr9:123630271-123632788CD8_primiary
SE_26718chr9:123629785-123632615Esophagus
SE_27931chr9:123630320-123632218Fetal_Intestine
SE_28718chr9:123630212-123631214Fetal_Intestine_Large
SE_30939chr9:123630434-123631230Fetal_Thymus
SE_39875chr9:123627352-123629663K562
SE_39875chr9:123630415-123631192K562
SE_50248chr9:123630276-123631237Sigmoid_Colon
SE_52520chr9:123630305-123631188Small_Intestine
SE_53449chr9:123629999-123632594Spleen
SE_55104chr9:123630521-123631203Thymus
SE_59300chr9:123630370-123667495Ly3
SE_59862chr9:123630341-123667956Ly4
SE_60687chr9:123630207-123668046DHL6
SE_61111chr9:123630545-123707493HBL1
SE_61770chr9:123630310-123667005Toledo
SE_62230chr9:123630172-123700621Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9123629631123629783
Number: 1             
IDChromosomeStartEnd
GH09I120865chr9123627353123629663
Enhancer Sequence
CATCTGGAGA GACAGAGGAG CCAAGGTCAG CCAGGACCAC ACCCCCAGTC AGGTATGAGC 60
TTCGGCAACC TTTCCCAAGT TAAATTTGCC CTCCACTGGC AGAAAGGGAA GAGAATTCAG 120
TTACTGAGCA CTTAGGCTGT GCCAAGGGAG GACCTGAGAG TTGGACATAT ACTCTCATTT 180
CACCTCACCA CCTGGTAAAA GATGGGACAC TGTCCCCATA TTACAGATAA GTCACAGGTG 240
AAATGGCTTG CCCTAGCTCA CAGGCAAGTG GAGGATGGTG ATTCAAATTC TGGTTTCCCT 300
AACTTCAGAG GCTGTGCTCT CCTTGCCATG CCACAATGAA GCCACCATTT CTGGACTTGC 360
TGCTTCCCAA ACACTGCTGA CAGGGAAACG TTTGCCTTGG AGACTTCACG GGAGAATAAT 420
GGTTTCTGTA AGCTGCACGG GGGCAAGACT ACATCTGGCT TTTCTCACCT GCAACTGTAT 480
CTGGCCTATC ATGGTCATCC AACAACTATT CATGGAATAT GAAGAGCAAA ATGCTCAATG 540
CTTCATTGAC ACCTTGTCAG GTGAGCTCCA GGTTAAAACG CAGATTCCTT GGTCCACTGC 600
AGACCTATTC AATCTTTGGG GAAGCCTCTG GGATGCATTT TTAACAAGCA TCCTGTGCAA 660
CTCTGCCCAT AGGCGTTGAG AAACACTGCA TTAATGCAGG AAAGGTTTCC ATAAGCATTT 720
CTCCATCTGA CAATACTTGG GGAAGCTCAT GGGCCTGAAG TTAAGGTTAA GCCCATTTGA 780
GAGATGAAGT AGTTCAAGCT TTGCCCAAGT TACCCAGCTG GAGCTTGGGG CTGAGATTCA 840
GGACTTCAGG GGGTCCTGAC GGCTGAACTT CCTGAGGGCA GAGACCCTCC CTCTTACATC 900
TGTGGTTCCT TCCACAATGC CACGTGCACT CAGCCCAAAG AAGCAAGCTC AACTGCCATG 960
GCTACATAGA GGCCCAGGTC GGCAAGGAAG AATCAAAGAC TCTTGCCGCA GAGCCAGGAC 1020
AAGAATTCCC TCCACAGTGG CCCCGACATA GCATGCCCCG CCCCCCGGCC CCCTACCCCT 1080
GCCTGATTGC ACATCTCCAG GGAAAAGAAT CTTTTCTATT TTTGGAGACA GGGTCGTCCT 1140
GCTTTGTCGC CCAGGCTGGA GTACAGTGGC ATGATCACAG CTCACTGCAG CCTCCATCTC 1200
CCAAGCTCAA GTGATCCTCC CACCTCAGCC TCCTACGAAG CTGGGACTAC AGGCGTGTGC 1260
CACCGCGCCA GGCGGGAAAA GGATCTTCAT ATCTCACCAG CAGCCGGTTC CACTGACTCT 1320
GACTGTGAAA AGGTTATCTT GACTTTCATG CATTAGTACC ACCACTACCA CCAGTAACAG 1380
CTCACATTTT TTTTGTTTAC CAAATGCCAG GCACTATGAG AACCTCTATG TGAATTACGT 1440
AATTCATGCT CTGCTCATAA TCACCACATG ATGGGGAAAC TATTCAGAGA GCTGAGGCTA 1500
AGGGGTTGCA CAGCTGGTAA GGAGCAGAGC TAGGACGTGG ACGTCCTGGG AGGATTCGCA 1560
CTGTGTCCGG CCCAGGCTCT TAACCACTCT TCAATACTTC CTCGTTTCCT ACAAAGCTCC 1620
AAGGTAACAC CTCTGCCCTC CAGCCCTGCT CCACAGTGCT AGATGCCACG CGGAGCCGGC 1680
CTTCTGTTCT CCCCTTGAGG TCCCGCCCCC TCGGGCCCCA CCCCGAGCCC TTCCCTTCAG 1740
GGACCGCCCC TTGAGGCCTC GCCTCCTCAG GTCCTGTTCC CGAGGCCTTA CTATTCCCTC 1800
CTCCCCACCC CGCCCCTCCA CAGGGTGCTT CTCGACCTGC 1840