EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS127-13854 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr17:74267380-74269860 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs193220chr1774268619hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr17:74268329-74268350TCGTCCTTTCAGTTTTGTTTC+6.05
JUNMA0488.1chr17:74268842-74268855ATGACATCATCAC-6.87
JUND(var.2)MA0492.1chr17:74268841-74268856CATGACATCATCACA-6.5
PLAG1MA0163.1chr17:74268774-74268788GGGGCCCAGGGGTG+6.27
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_10428chr17:74261317-74270738CD19_Primary
SE_11415chr17:74257434-74273567CD20
SE_15056chr17:74267081-74270069CD4_Memory_Primary_7pool
SE_18937chr17:74266584-74270083CD4p_CD25-_Il17-_PMAstim_Th
SE_19565chr17:74266473-74269954CD4p_CD25-_Il17p_PMAstim_Th17
SE_21340chr17:74266682-74269376CD8_Memory_7pool
SE_23599chr17:74266807-74269354Colon_Crypt_1
SE_24131chr17:74267376-74269109Colon_Crypt_2
SE_24131chr17:74269228-74269783Colon_Crypt_2
SE_24931chr17:74266871-74269172Colon_Crypt_3
SE_24931chr17:74269202-74271077Colon_Crypt_3
SE_27367chr17:74266689-74270067Esophagus
SE_28090chr17:74257585-74269455Fetal_Intestine
SE_29152chr17:74254176-74269372Fetal_Intestine_Large
SE_31864chr17:74264958-74270935Gastric
SE_32663chr17:74261503-74269696GM12878
SE_43246chr17:74266783-74271643Lung
SE_47749chr17:74267413-74269184Pancreas
SE_48284chr17:74258480-74271528Psoas_Muscle
SE_50371chr17:74266677-74270078Sigmoid_Colon
SE_52552chr17:74254274-74270056Small_Intestine
SE_53757chr17:74260072-74269790Spleen
SE_55588chr17:74267363-74269873Thymus
SE_58966chr17:74257592-74273389Ly3
SE_60322chr17:74239092-74270751Ly4
SE_60510chr17:74247565-74275632DHL6
SE_61026chr17:74257641-74276199HBL1
SE_62440chr17:74241844-74272934Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr177426906074269291
chr177426900074269808
Enhancer Sequence
CTGGTTTGCG GTGCTTTTAT TTCCGTTGGT GGGAAAAGCG GTCTCCTCAG AAGAGGGGTG 60
GTGGGGGTCC CTTGCCACTG GGCTGGTCTG GATGTTTTTG CTGTGGGATG GTCACACCAG 120
GGGCTCTGAC AGCAAGGTCC AGGTTGGTGT GGGGAGGAGA GAGGGGCCGG GGTCCGTCCT 180
GAGTTTCTGT GACCTTCCCT TCTTGGCCCC ATCGGTGTAG CCCCCACCCA CAGAGCCCTA 240
GTGAGAAGAG CTGGAAGCCA TTTTCATCTA CAGTGGGGAG AGCTTCCTTC TAGCTGGGGG 300
CCTCCTGATG GCCCCCCCAG GCCCTCCCAG GAAGCATCTT CCAGCTGGGC TCATCTCCGA 360
TACTCCTCTC CTCAGCTTCC CGGGGGCAGT ATGTCCCTTT GGGTCATGGC CTGTGGAGTG 420
GCCATGACCC AAAGTTCAAT TAAGGCTGGC GGGTCCCCAG AGGGGCCTGC TTCCATTCCC 480
CCTTCCCCGC AGCCCTGCAG GCGTCAGCAT GGGGCGAGGT TACCAGTTCC TGACCCAGCA 540
GCTCGTCCTC AGGTGGTCCT GCTGCTCGGG AGGTCAGCTG CGTGGGGAGC CTGTCCACCT 600
GGCTGATGGG GGTGATGGCC GCGTGGCTGG GATTCCTCCT CCAGCCCTGC CCTTCACCGC 660
CATACAGTCT GGGCAGCCCC TTCCTGTCCC GTCCTCCTGC CTCGCCCTCT GCTGGGGTCT 720
ACGGGGCCCA AGTCTTGCTG GAACACAGGC AGGACAAGGG TTCTGGAGGT TCAGGCCGGA 780
AGTGAAATAA AAGTCGAGAG GGGCCGGGCC CGGCACCCAC CGCATCCTGC CTCCGGGCCT 840
CCTCGGGCCC CTCACACGGT GGGGCAGCCC CTCCTCCAGT GGAGCGGAAC GGTGGGCCCC 900
GCTGCCCCTC CACCCCTGCG TGTGACACGG ACGTGCTTGG AAGCTGGGTT CGTCCTTTCA 960
GTTTTGTTTC CTGGTTGGAA ACCCCTGAGA CTCCTCCCCC TCCCCCCGCC CCTGCCCACC 1020
TGTGCTTTCC CAGGCTGGAA GGGGCAGCCC CTCTCAGCAC GTGGGTGGTT AGGCTGTGAC 1080
GTCCCCAGGC CTCCTGGGCC TGCACCGGGG TCCACCCAGG TGTGGGCCAT GCCCAGGTGC 1140
GGGAATGGTC GGGGGTTGCC CTGGCCGGCT TAGGGAATGT CGCTCTGGGA CCTTCTGTGG 1200
GCGTGGGGAA GGCCTGGGTG AGGAGGGCTG GGCTGCACCT CCCTGCCAAG CTGGTGAATT 1260
TGGCTTCTAG ACCCGGGAAA CTGAGCCACC TTCTGACATT TCACAGCCAG GGTGGGGCCG 1320
AGAGCAACAG GAGCCCAGCT GGAGCCTGGG AGGGGTGGCC CTGCCTCTGC CTCCTGCCCG 1380
GGGAGAAAGG GGCTGGGGCC CAGGGGTGCC CGCCCGGGGC TCCGCTGTCT GAGCAGCTCC 1440
TCTCTTCTGT CCAGCTCTGA GCATGACATC ATCACATGAA GACTCCCAGG GTCTCTGAAG 1500
AGCAGGCCAG GAGGGAGCGG CCACCCGACC CAGCCAAGCC TGCCCCGCTT TGCCCACGCG 1560
GGGGTCAGGG GCCAGAAACC TGTTTCTGGG CTGTTTCTCG CCACATTTTC CTTTCCTGTG 1620
TGATTTTGTC TCCTCACACC CCAAAGCGGG CCTCTTACTC TAGACATCCC TTTCCCATGC 1680
TGGGGAGATG GGAACTGGGG GTGGGGGGAG CCCCTTTGTC AACTCTGAGC ACTTCCTTTT 1740
CTCTGAGGAG GGAGCCTCTG AGGCAGAAAG GCTTTGGTGA CCTCAGGGCT TTATAAACCT 1800
CAGGGTGGGG GGGCCACTCT CATCTACTGG GGGACCCCTA GAATCTGGCT GGAGCCCAAG 1860
CTCAGGAGGT CAGGGGACTC CTTGGTCTCA GGAGCTTCAA GTGGGTTGCA GCAGTGATAG 1920
GGGCTCGTCT CTAGCAGTTG CTGCACTGGC CCAAGCTCAG TCTCACTTGC AGTCCTCTGT 1980
CCCCTCACCT GCCAAGACCT TTAGTGAGTC CCTTGCCTGC AGGTGTTGGG GCTAGGGCAG 2040
AGGGAAGCAA ATCACAAGCG ACAAGCGCCA GGCTCGCACC ACCTCTCCAC CCGCCGCCTG 2100
GATGTCTTTT TCTAGGAGGG GAATGGGGAA ACTGGGTCAC AGCCACAGCA GCCCCTGCTC 2160
TGTGCCTTCA GGCCCCGGCT GTCTCTGCAG CAGCCCACTC AAGGGAGAGA AGCGGAGGGC 2220
GGCAAACAGA AACCTGCCCA GCCGGCTGCA GGGGTTCGCC TCCAGCCATT GGCACTGCTT 2280
CCCCGGAATC CCACGCCAGG GGTCAGGAAC CACCCTGAGC CAGCAGCAAG AGCGCAGCAG 2340
GCAGCTGCCA CCCTCACCCC CAGAGTGCTG GACACTGACA GCACGGGCCC CAGCACCCCA 2400
GGCTAGAAGG CAGGTCTAGA GCCAGAAGGC AGGGCACCCC CAATCTAGCT GAGGCCAGGA 2460
GAGAGCTGGT GGGGTGAGCA 2480