EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS182-21463 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr9:33129080-33131810 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SPI1MA0080.4chr9:33129997-33130011TAAAAGAGGAAGTA+7.06
SPICMA0687.1chr9:33129997-33130011TAAAAGAGGAAGTA+7.73
ZNF263MA0528.1chr9:33129892-33129913GGAGGAGGAAGTGGCTGGAGG+6.59
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_00330chr9:33131315-33133010Adipose_Nuclei
SE_09459chr9:33129171-33132533CD14
SE_10229chr9:33127769-33131935CD19_Primary
SE_10912chr9:33119344-33169982CD20
SE_12090chr9:33130620-33131585CD3
SE_18665chr9:33129793-33132844CD4p_CD25-_Il17-_PMAstim_Th
SE_19329chr9:33130392-33131632CD4p_CD25-_Il17p_PMAstim_Th17
SE_20045chr9:33128349-33132443CD56
SE_22416chr9:33128783-33132526CD8_primiary
SE_26031chr9:33129309-33132935Duodenum_Smooth_Muscle
SE_26859chr9:33129122-33131571Esophagus
SE_27770chr9:33128137-33132419Fetal_Intestine
SE_28724chr9:33128066-33132484Fetal_Intestine_Large
SE_31534chr9:33128891-33131746Gastric
SE_32659chr9:33129028-33131615GM12878
SE_35029chr9:33129460-33130398HeLa
SE_35029chr9:33130436-33131878HeLa
SE_40894chr9:33128725-33131858Left_Ventricle
SE_41831chr9:33129685-33130482LNCaP
SE_41831chr9:33130578-33131658LNCaP
SE_42236chr9:33128546-33131800Lung
SE_44340chr9:33130634-33131475NHDF-Ad
SE_45731chr9:33130368-33132932Osteoblasts
SE_47814chr9:33129311-33130060Pancreas
SE_48738chr9:33128803-33130531Right_Atrium
SE_48738chr9:33130653-33131691Right_Atrium
SE_50176chr9:33128355-33131838Sigmoid_Colon
SE_52621chr9:33128937-33131899Small_Intestine
SE_53402chr9:33129123-33131619Spleen
SE_58985chr9:33124740-33168862Ly3
SE_62118chr9:33106994-33169093Toledo
SE_62346chr9:33106942-33169226Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr93312960033131200
chr93312952733131297
Number: 1             
IDChromosomeStartEnd
GH09I033127chr93312796433132882
Enhancer Sequence
TTCAGGCAGG CTCCAGCTCT GCTTCCTGGC CATCGTGTGC TTACCTGTGG AGCCTTCCCT 60
CTGCAGGAAC AATCAGAAGA CCATTTGCCT TACTCTGGGG GATGGGGGGA GGTGGGAGGT 120
TCAAAATTCA AAGTGAGACC ATAAAGGTGC TGAGTCCAAA GGACCCTAAA GGAGTTTTGT 180
GACCATTAAC AATCACAAGG CTAAGGTATT AATAGGTTTT CTGCATTTTT CCTGATAAGG 240
GAGGTCACCC CAAGGACTGT CACAGGCAGC CTGTGCTCTG GTCAGCATTG AGCTGGAAGC 300
TTCGGGGAGA GGCCCAAGGG AGGGATCCTG CAAGTTCCCA AGGGTCAGGA CCTGGCCCCA 360
CTGGGAACGG AGGCTTCACT TCCAAGAGGC ACAGATTTAG GCAGAAGACC AGGAGTAGGG 420
AGTCCTGAGA CTAGGGATAA ACAAAGGGGC AGGAATCCTG GAGAGAAGCC CCGTGCTCCA 480
CTCACTGACT GCGTCTGTAC TGACTATGTA CCAGCTGTGT GGTCAGAGAG AAAGAAGGGA 540
GGCAGACATG AGGGACTCAG AGTCCGGGGG CTGGGGTGAG GCTGGAACTC AGATAATCAT 600
CCCTTTCCAG AAAGTTCTGA GCAGCCTGGG AGCAGCAGGG AAGGAGAAGT CAGCTCTATT 660
CCAGGGGCTC CACAGAACTA ATGAGGTTGG GGAGGGAAGC TTAAAAGATA GCCAGAGACA 720
CACTAGGAAC ACAGGGGACA GCATAAGCAA AGGCACACAG AGGGGAGAAC AGAGGTGTCT 780
GGGTGGAGAT GGGGAGTCCA GTGAAGTGGA GAGGAGGAGG AAGTGGCTGG AGGTAGGTCA 840
GGGTCTCGGA TGCTAAGCTT GGGCCTTCCG ACCATTTAGA CCGTTGCCTG TAGGCAGTCG 900
TGAAATGCTA ACAGGTTTAA AAGAGGAAGT AACATGGTCA GAACCAGAAA AATCCTGGGC 960
AGCTGAGGGA GAGGAACAGA GGTGCCAGAA GATATGCAAT CGGAATTGGA GAGACCAGTT 1020
CTGTGTACTG GCTGTGGGGC AAAGGGCTGC CATGGTTGTG ACAAACCCAC CTGGCCAGCT 1080
GTGCCTGCAT TCCTTACTCA TTTTGTAATT TTTATGATGG GCAATCCCAC AAACATTCTG 1140
CATTCCTTAA TTTAGGGCTA GTGCTACCAG GTGGTGACCT GCCCTCCCTT CACCTTGAGT 1200
GAAGTCTCGT TTCCGGGTTT GAGTATTAGG AAATGCAGCA TGCATCCCTG TTTGCTATGA 1260
TGTCTTCTCC TTCTGTTGCT TCTTTTCTTG CTGCCGTTGA AGTTGGAATG CTATATCTTG 1320
AAATCCACGT CTCAGAGTAC AAGGAGTCAA ATAGTATTCT CCCATGCTGG TGAGCTAAGG 1380
TCAGGGGTGG GAGGAGAGAC CTTAAGGAAA AAGAGCAACT CTTGTTCTTC TATATCTCAA 1440
CCAGGAAAGC CTCTCCCGGC TCATTCCTTC AATATCCTTA TTTTAAGATA TAAGTTAGTA 1500
CAATAATTAC AGAGGCATAA GCCAAATGGG AGTGGTTAAC AGCTTACTAT AGACAGAGTA 1560
TGAGTCATAA CAACTTGTGA AAGTTCACTC CTGTGTGTAA AGCTTGATAC GTGGCCCTAT 1620
TTTGAAGAGG CTTATAGGCC CGGGATGGCC TCTGAGATTC TGCCACCTGG CTCACTCCAC 1680
TATCCATTAC CCTCTGACTC CAAGGAGTTC AAACCAATAG GAGGAAGGGT CCTGATGCGG 1740
GCCCTGAGTG GGGGTGCAGC AGGAGGCGGT GGGAGCCATG AAGAATTCAC CACCACAGAA 1800
GCAGGCAGAG GAAGCAGGCA GAGGAAACAG GCAGGATGAA TGGAGAGTGG AGAGGCAGGA 1860
GTGGACCCTC CTAGTAACGG CTGGTATTTA CTGAAGGTTT ACCATGAGAA GGATGCCTCA 1920
TAACCCTCCC CACCAAGGAG GAAACTGAGG CCTGCAGAGC TTAAGTAACC TGCCTGAGGT 1980
CACTGACTGT AAAGTGGCAG TGCCAGGACT GAACCCAGGC AGTCTGAGCA CACAGCACAC 2040
TCTCAGCCCT GGATACCAGA CTGTGAGCAA CACTGGGGGC ACCCTGGCCA TGAGGAGTGT 2100
CACTGATGCC CTGAGAAGGC ACTAAACCTG GAGTCAGACG CTGGGGTTTG AGCCGCAGCC 2160
CTACTGTTGT CTATGTGACT TTCGGAGCCT GTCCCTCTCT GAGCCTGTTT CCTCACCTGT 2220
GACATGGAGC AGAAGTTTCT ACATTGTCTG GCCTCAGGGG TCTAGGCAAA TCCTAGCAGT 2280
GACTGAATGG GAAGCCAAGG AAGTGGAAAT GGGACATGGC CCCTACTTCA AGTAGAATGA 2340
AACCCTTGTG ACCTGCTGTA AGCGGAAGGT TGTGTAGCAT TTCAATGGGG CAGAAAGAAA 2400
TCTGATACTG AAAAGCCTGT TTGGGAACCC TTGGACTAAA TGTCTCAGAA GCCACTCCAT 2460
TTTGAGCATT ACTTCTGTCT AATCTTAAAT GGTATGTGTG TGTGTGTACA TGTGTGTGCA 2520
TGTGTATGTG TGTGTGGGAA TGAAAAGTCA AAATGACAGC AGGGTGTCTG GGCCAGGGAT 2580
AAGCTGAGAG GCTATAAAGA GGGCTAACAG CCCATAAGGT TTATTTGCTC AACAAACAGT 2640
GCAGAAAGGT CAAAACCAGG TGCTACAAAA TCCCTTTCTT CTTCTAGAAT ATAACCATAA 2700
AACAGATAAC ACAGGCAGTT CCTAATTTGT 2730