EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS017-33781 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr9:123629320-123631080 
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
TAAATTTGCC CTCCACTGGC AGAAAGGGAA GAGAATTCAG TTACTGAGCA CTTAGGCTGT 60
GCCAAGGGAG GACCTGAGAG TTGGACATAT ACTCTCATTT CACCTCACCA CCTGGTAAAA 120
GATGGGACAC TGTCCCCATA TTACAGATAA GTCACAGGTG AAATGGCTTG CCCTAGCTCA 180
CAGGCAAGTG GAGGATGGTG ATTCAAATTC TGGTTTCCCT AACTTCAGAG GCTGTGCTCT 240
CCTTGCCATG CCACAATGAA GCCACCATTT CTGGACTTGC TGCTTCCCAA ACACTGCTGA 300
CAGGGAAACG TTTGCCTTGG AGACTTCACG GGAGAATAAT GGTTTCTGTA AGCTGCACGG 360
GGGCAAGACT ACATCTGGCT TTTCTCACCT GCAACTGTAT CTGGCCTATC ATGGTCATCC 420
AACAACTATT CATGGAATAT GAAGAGCAAA ATGCTCAATG CTTCATTGAC ACCTTGTCAG 480
GTGAGCTCCA GGTTAAAACG CAGATTCCTT GGTCCACTGC AGACCTATTC AATCTTTGGG 540
GAAGCCTCTG GGATGCATTT TTAACAAGCA TCCTGTGCAA CTCTGCCCAT AGGCGTTGAG 600
AAACACTGCA TTAATGCAGG AAAGGTTTCC ATAAGCATTT CTCCATCTGA CAATACTTGG 660
GGAAGCTCAT GGGCCTGAAG TTAAGGTTAA GCCCATTTGA GAGATGAAGT AGTTCAAGCT 720
TTGCCCAAGT TACCCAGCTG GAGCTTGGGG CTGAGATTCA GGACTTCAGG GGGTCCTGAC 780
GGCTGAACTT CCTGAGGGCA GAGACCCTCC CTCTTACATC TGTGGTTCCT TCCACAATGC 840
CACGTGCACT CAGCCCAAAG AAGCAAGCTC AACTGCCATG GCTACATAGA GGCCCAGGTC 900
GGCAAGGAAG AATCAAAGAC TCTTGCCGCA GAGCCAGGAC AAGAATTCCC TCCACAGTGG 960
CCCCGACATA GCATGCCCCG CCCCCCGGCC CCCTACCCCT GCCTGATTGC ACATCTCCAG 1020
GGAAAAGAAT CTTTTCTATT TTTGGAGACA GGGTCGTCCT GCTTTGTCGC CCAGGCTGGA 1080
GTACAGTGGC ATGATCACAG CTCACTGCAG CCTCCATCTC CCAAGCTCAA GTGATCCTCC 1140
CACCTCAGCC TCCTACGAAG CTGGGACTAC AGGCGTGTGC CACCGCGCCA GGCGGGAAAA 1200
GGATCTTCAT ATCTCACCAG CAGCCGGTTC CACTGACTCT GACTGTGAAA AGGTTATCTT 1260
GACTTTCATG CATTAGTACC ACCACTACCA CCAGTAACAG CTCACATTTT TTTTGTTTAC 1320
CAAATGCCAG GCACTATGAG AACCTCTATG TGAATTACGT AATTCATGCT CTGCTCATAA 1380
TCACCACATG ATGGGGAAAC TATTCAGAGA GCTGAGGCTA AGGGGTTGCA CAGCTGGTAA 1440
GGAGCAGAGC TAGGACGTGG ACGTCCTGGG AGGATTCGCA CTGTGTCCGG CCCAGGCTCT 1500
TAACCACTCT TCAATACTTC CTCGTTTCCT ACAAAGCTCC AAGGTAACAC CTCTGCCCTC 1560
CAGCCCTGCT CCACAGTGCT AGATGCCACG CGGAGCCGGC CTTCTGTTCT CCCCTTGAGG 1620
TCCCGCCCCC TCGGGCCCCA CCCCGAGCCC TTCCCTTCAG GGACCGCCCC TTGAGGCCTC 1680
GCCTCCTCAG GTCCTGTTCC CGAGGCCTTA CTATTCCCTC CTCCCCACCC CGCCCCTCCA 1740
CAGGGTGCTT CTCGACCTGC 1760