EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-09571 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr21:45594630-45596630 
Target genes
TF binding sites/motifs
Number: 20             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr21:45595440-45595458CTTTCCTTCCTTCCTTCC-10.53
EWSR1-FLI1MA0149.1chr21:45595460-45595478CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr21:45595432-45595450TTTTCTTTCTTTCCTTCC-6.18
EWSR1-FLI1MA0149.1chr21:45595480-45595498ACTTCCTTCCTTCCTTTT-7.06
EWSR1-FLI1MA0149.1chr21:45595464-45595482CCTTCCTTCCTTCCTAAC-7.74
EWSR1-FLI1MA0149.1chr21:45595472-45595490CCTTCCTAACTTCCTTCC-7.83
EWSR1-FLI1MA0149.1chr21:45595468-45595486CCTTCCTTCCTAACTTCC-7.92
EWSR1-FLI1MA0149.1chr21:45595476-45595494CCTAACTTCCTTCCTTCC-8.06
EWSR1-FLI1MA0149.1chr21:45595436-45595454CTTTCTTTCCTTCCTTCC-8.46
EWSR1-FLI1MA0149.1chr21:45595456-45595474CCTCCCTTCCTTCCTTCC-9.42
EWSR1-FLI1MA0149.1chr21:45595444-45595462CCTTCCTTCCTTCCTCCC-9.47
EWSR1-FLI1MA0149.1chr21:45595448-45595466CCTTCCTTCCTCCCTTCC-9.6
EWSR1-FLI1MA0149.1chr21:45595452-45595470CCTTCCTCCCTTCCTTCC-9.83
ZNF263MA0528.1chr21:45595436-45595457CTTTCTTTCCTTCCTTCCTTC-6.03
ZNF263MA0528.1chr21:45595432-45595453TTTTCTTTCTTTCCTTCCTTC-6.1
ZNF263MA0528.1chr21:45595443-45595464TCCTTCCTTCCTTCCTCCCTT-6.28
ZNF263MA0528.1chr21:45595456-45595477CCTCCCTTCCTTCCTTCCTTC-6.76
ZNF263MA0528.1chr21:45595440-45595461CTTTCCTTCCTTCCTTCCTCC-6.92
ZNF263MA0528.1chr21:45595448-45595469CCTTCCTTCCTCCCTTCCTTC-7.12
ZNF263MA0528.1chr21:45595452-45595473CCTTCCTCCCTTCCTTCCTTC-7.39
Number of super-enhancer constituents: 21             
IDCoordinateTissue/cell
SE_03880chr21:45594629-45595412Brain_Anterior_Caudate
SE_05779chr21:45595345-45598232Brain_Hippocampus_Middle
SE_06690chr21:45594579-45596553Brain_Hippocampus_Middle_150
SE_09453chr21:45594378-45596588CD14
SE_10160chr21:45592165-45598304CD19_Primary
SE_10883chr21:45590077-45601846CD20
SE_24239chr21:45595736-45596761Colon_Crypt_2
SE_31647chr21:45595665-45596690Gastric
SE_33667chr21:45595623-45597713H2171
SE_50113chr21:45594632-45595380Sigmoid_Colon
SE_50113chr21:45595470-45597809Sigmoid_Colon
SE_52463chr21:45594654-45595187Small_Intestine
SE_52463chr21:45595535-45597270Small_Intestine
SE_53405chr21:45594659-45595253Spleen
SE_58720chr21:45552566-45596359Ly1
SE_59125chr21:45557380-45640832Ly3
SE_60477chr21:45556693-45597600DHL6
SE_61237chr21:45557180-45641526HBL1
SE_61527chr21:45545883-45641600Toledo
SE_62281chr21:45556124-45641130Tonsil
SE_65639chr21:45594799-45597491Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr214559600445596289
chr214559464645595455
chr214559565245596342
chr214559635445596450
Number: 2             
IDChromosomeStartEnd
GH21I044169chr214558978945597483
GH21I005084chr214559492845597452
Enhancer Sequence
ATTTATTTAT ATTTTAAGGG GGATTTGAGA AACTGAAAAA CACGACAGCA CCCCTCATAG 60
GCGACTTTAC CCAATAAAGT CGGTGATCAT AACATTTTCT CCAGCACAGA CACACAGGTG 120
TGCTCATTCA GTCACGTGGA TATGAGTTAT GTGCAGATGA ACCATTCACA GAGAAACTGG 180
TCAGAACACC AACATGTTAG GTTTTGATCT TTCAGGAGCT CAGGATTTGG GATGACGGTG 240
TTCGGGGTCA GGTCTTTTGA GGTTCTGATC AGCGCCGCCT CACCGCGCGA TACCAGTGCA 300
GAACGGGGAG ACCCAGGTCG TCCAGGAGCT GGACTCCAGC CGGGACAGTC TGTCTGTGTC 360
AGAGCCCGGG TCCCTCATGG GGCACTCAGC CTTCACTCGG GTTTCCTGCA AAAATGGAGA 420
GCTTTTTTTC AAGTAGGGAT GCCAAGGATG GCAGGCATGA AGCGGGCAGG CAGAGGTGGG 480
AGCTAGTTAG CAGCATCTCC AATTACCGTG ATGGGCAGAA AGAAGGTTCT AGACAACAGT 540
GTCTTGATGA GGTCAAGAGG AACTGAAACC CCCACCCCAC TTCCCCTGCC CCATCTGGTT 600
CTGGGAAAGG GGAAATGCAG GTGCCGGCTG TGCGTGGGTC AGTGGCCCGC CCCCGCCTCT 660
CTGCCTCGCG GACGTCCAGA CTTCCGAGGC CTGGCTGTCT GCAGGGCGGC CATTGCTGTG 720
CGCGCGCGCG CGGGCATGTG CATGGTTCAG GGAAGAGGCT GCATTTCACA GAGACTCTGT 780
CCCAGGAGGT AGGCATTTTT TCTTTTCTTT CTTTCCTTCC TTCCTTCCTC CCTTCCTTCC 840
TTCCTTCCTA ACTTCCTTCC TTCCTTTTTC TTTCTCTCTC TTTTCTTTTC TTTCTTTCTT 900
TTTTTTTGAC AGAGTCTTGC TCTATCGCCC AGGCTGGAGT GCAGTGGCGT GATCTCGGCT 960
TATTGTAACC TCCACCTCCC AGGTTCAAGC AATTCTCGTG CCTCAGCCTC CTGAGTACCT 1020
GGGACTAGGG GTACGCACCA CCACGCCCAG CTAATTTTTG TATTTTTAGT AGAGATGGGG 1080
TTTCACCATG ATGGCCAGGC TGATTTCGAA CTCCTGGCCT TAAGTGAGCC TCCTGCCTCG 1140
TTCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCATG CCCAGCCGGC ATTTTCATCT 1200
GGACTCTGCC ATGGGGCTCA GCAAATCAGA TGTGACCTGG TGACAGGTGC CAAGAAGGTC 1260
TGGCGACCAC AGGTTTCTTG TCGGTTTCTG CCTGGGACCC CCGCACCTCC CTACCAGTAT 1320
TCCCAACCCA ACGAAAGACC GGCCAAGTAC AAACCAAGGG CAGCCCTGAA GCCCAGGACC 1380
ATGAGGCCTG GAAGGCCCCA GGACAGGTGA TTTGTGGCCC TGGTGTCTCA GGTCAGGAGC 1440
AGGGCAGAGC CACCTTCCTC CCTCCCTGTG CGGGGCTGCA TGAGCTCAGG GACCTTTGGA 1500
CCTGAGAAAG GTCAGGCTCA CTTCCTCCCC GTGCCTGCGG TTGGCCGCAG GGGGAATATT 1560
CTCCTGACCC GAGTCCCGAA GCCCTGGGCG TGGAGTTTCC CTGGACTGGG AGAAAGTAAA 1620
CACCGAGGGA CTTGCCAAGA GGAAATGGAG AAGCCCAGGT GTTCTGGGCG GAGCTGAGTG 1680
TCCCGCAGGG GGTTCCGCAG CTCCTCGCCT CTGGAAGACC AAGGACAGCT TTCCCCAGGG 1740
CTACAGCCTC ACGCTCCCCT CCCATCGTGG CTGGGCCTTT ACTTGGGGGT GAGTGTCCTA 1800
CAGACGAGGG GCTTAAAGCT ACAGGAATGC CTCGTCTCGC AGAGCTGGAG GCTGGAAGGC 1860
AGATCGGCCT GTGAGGGCCG CGGTCACTCT TGGTCCTGAG CCCTCCTTGT CCGGCTGCTG 1920
GTGTCACGGG CACTCCTTGG GGTTCCTTGG CTTGTGGGAG CATCGCGCCG GCCCCGCCTC 1980
TGTCATCAGG CCGCCTCCCC 2000