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

TagContent
EnhancerAtlas ID
HS182-04596 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr11:130033390-130034260 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CEBPAMA0102.3chr11:130034088-130034099TATTGTGCAAT-6.62
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_09333chr11:130032381-130034533CD14
SE_23084chr11:130029095-130034455Colon_Crypt_1
SE_23752chr11:130033318-130034120Colon_Crypt_2
SE_24749chr11:130032875-130034411Colon_Crypt_3
SE_27111chr11:130029500-130034306Esophagus
SE_27706chr11:130028973-130034575Fetal_Intestine
SE_28552chr11:130028860-130034626Fetal_Intestine_Large
SE_41707chr11:130033390-130034091LNCaP
SE_50138chr11:130029120-130034564Sigmoid_Colon
SE_52428chr11:130029080-130034495Small_Intestine
SE_57437chr11:130032964-130034100VACO_503
SE_58202chr11:130032963-130034221VACO_9m
SE_58488chr11:129985075-130060331Ly1
SE_60756chr11:130015852-130052711DHL6
SE_61683chr11:129986883-130083431Toledo
SE_65550chr11:130028561-130034237Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11130033861130034000
Enhancer Sequence
TCCTTGTCTC AGACTTCTAA GTAGTTGGGA TTACAGGCGT GAGCCACTGT GCCCACATAA 60
AACTTTAGAG AACTGCCTTT TTTGTTCTCT AGAGCATGTG CTGGGCAGGT GTGTGCAGTG 120
GGTGAGGAAG AGGGTTGGGA AGGCAGAAAG CAGCAGGAAG CTAGGATTGT CCTGTAGGTG 180
GGGCTTCAGC TGCTGGAGTG GACCGGAAAT CTGCCTTCTC CAGGGGCTTT CTGGAGCCTT 240
CCCTCTGCCT TGGTCCTGAG AACACCTGGA AATTCCTCGT TTAGGAGTTG AGAAAACTGA 300
GGAAGAGGAG AAGATGCCCC TAGTTTGATG GCTGCCTTCG CCTGCTAGCA GTGGAAATGG 360
TCAGAGGGTG GACCTGCTCG AGCCGACTTG CTGGCCTGTT GCCACGTTGT CACCGGCTGC 420
GGAAGGAGAA CGAGTCACAG CTCCCTCCCC CTACCTGACC CTCACTCTGC TCCCTGGGAA 480
CCAGACTACC AGACTGCCTA CTGCTGTGGC CAGTGGCTTC TGTCCCTCGG AACACTGTGG 540
CCCTCAAGTT CCCTGATGTC TGCTCCTTCT CTGGTCTGTG GTTCTGCCAA GGCTGGTGGC 600
TCATGTCTCT TTTAAAAGAG AAGTTGTCTT TGGAAGAGGA AGGGAAACGT GACAGAGTCC 660
CCTGGGAGCC CAGGTCCTGA AGATGATGTT GCTTCTGATA TTGTGCAATG ATTACTGGAG 720
TGTCTAGAAT ACTAATAATG ATGAACACTA ATAATCGTTA GCATTTATTG AGCATGGCTG 780
GCTGCTTGTC TTTTTTCCTG CCAAGCTTCA TTGAACTAAC TGTGTACCTA GTCCTGGGTC 840
AGGCATGGCT GAAGGGAAGT AAGATGTGGT 870