EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS053-24966 
Organism
Homo sapiens 
Tissue/cell
Foreskin_keratinocyte 
Coordinate
chr21:34753810-34756640 
TF binding sites/motifs
Number: 20             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr21:34754590-34754608GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr21:34754594-34754612GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr21:34754670-34754688AGAAGGGAAGAAGGAAAG+6.03
EWSR1-FLI1MA0149.1chr21:34754578-34754596GAAAGGGAGGGAGGAAGG+7.45
EWSR1-FLI1MA0149.1chr21:34754582-34754600GGGAGGGAGGAAGGAAGG+8.32
EWSR1-FLI1MA0149.1chr21:34754598-34754616GGAAGGAAGGAAGGAAAA+9.07
EWSR1-FLI1MA0149.1chr21:34754586-34754604GGGAGGAAGGAAGGAAGG+9.47
Foxd3MA0041.1chr21:34756589-34756601GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr21:34756593-34756605GTTTGTTTGTTT+6.32
IRF1MA0050.2chr21:34754551-34754572AAAAAAAAAAAGAAAGAAAGA-6.25
Klf1MA0493.1chr21:34756066-34756077AGCCACACCCT+6.02
Nr2f6(var.2)MA0728.1chr21:34754336-34754351GAGGTCAGGAGTTCA+6.22
USF1MA0093.2chr21:34755676-34755687GCCACGTGACC+6.62
USF2MA0526.2chr21:34755674-34755690GCGCCACGTGACCCAG-6.69
ZNF263MA0528.1chr21:34754580-34754601AAGGGAGGGAGGAAGGAAGGA+6.09
ZNF263MA0528.1chr21:34754575-34754596GAAGAAAGGGAGGGAGGAAGG+6.23
ZNF263MA0528.1chr21:34754595-34754616GAAGGAAGGAAGGAAGGAAAA+6.56
ZNF263MA0528.1chr21:34754591-34754612GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr21:34754584-34754605GAGGGAGGAAGGAAGGAAGGA+7.08
ZNF263MA0528.1chr21:34754587-34754608GGAGGAAGGAAGGAAGGAAGG+7.42
Number of super-enhancer constituents: 14             
IDCoordinateTissue/cell
SE_00219chr21:34750982-34756583Adipose_Nuclei
SE_09780chr21:34750609-34758167CD14
SE_10653chr21:34751101-34757835CD19_Primary
SE_10924chr21:34750502-34759616CD20
SE_27036chr21:34753764-34754350Esophagus
SE_27036chr21:34754548-34756615Esophagus
SE_36753chr21:34750915-34754406HMEC
SE_36753chr21:34754454-34756616HMEC
SE_53413chr21:34751185-34757173Spleen
SE_58466chr21:34731200-34786233Ly1
SE_60169chr21:34732700-34761220Ly4
SE_60632chr21:34732666-34757447DHL6
SE_61512chr21:34731229-34778660Toledo
SE_64665chr21:34754499-34756570NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr213475470834755048
chr213475529634756154
Number: 1             
IDChromosomeStartEnd
GH21I033378chr213475110834757769
Enhancer Sequence
AGGCATGAGC CACCACATCC AGCTAATTTT TTTTTCTTTT TTTTTTTTGT AAAGATGGGG 60
GTTTCCACAT TGCCCAGGCT GGTCTCAAAC TCCTGGGCTC AAGTGATCCA CTGCCCTCGA 120
CCTCCCAAAC TGCTGGGTGC TGGGATTACA GGCGTGAGCC ACCACTCCCA GTCTAGGGGC 180
CCACTTTCGA ATCACAAGCA GCCACTTTCT GGAAGGCACC TCATCACGCA TTGGCAGGGC 240
TATGTCCCTC ACAGGTTGCC CCAGATGACG GTCTTCCCAA GTGACTTCTG CTCCAGGTCC 300
ACTGTTCAGG CTCCCCTTGG TCCTACCCCT CCAGACATCC AGCCTTGGGG GGATCCTGGG 360
CCCCTACTGT TCTTTCCTAT ATCAGCCTCA GCCAAGCTCT CCTCACCCCT CAATCCATCA 420
GATGTCCTCC AGTGACATTG AACTTCAAAG AAAGAGCAGA GGCCAGGTGT GGTGGCTCAT 480
GTCTGTAATC CCAGCACTTT GGGAGGCTGA GGTGAGTGGA TCACCTGAGG TCAGGAGTTC 540
AAGACCAGCC TGCCCAACAT GGTGAAACTC TGTCTCTACT AAAAATACAA AAAAATTAGC 600
CGAGCATGGT GGCGGGCACC TGTAATCCCA GCTACTCGGG AGGCTGAGGC AGGAGAATTG 660
CTTGAACCTG GGAGGTGGAG GTTGCAGTGA GCCGAGATTG TGCTACTACA CTCCTGCCTG 720
GGCGGCAGAG ACCCTGTCTC AAAAAAAAAA AAGAAAGAAA GAAAAGAAGA AAGGGAGGGA 780
GGAAGGAAGG AAGGAAGGAA GGAAAAAGAA AAGTAAAGAA CAGAAAAAGA AGAAAGGAAA 840
AGAAAAGAAA GGAAAAGAAA AGAAGGGAAG AAGGAAAGAG CAGAGAGGCC CAGTCGCTCT 900
TCTCAGAGTC TCCGTGGCAT CTCGGTAGAT TTGCTGATCC CTTTACATAA CCCAAGTTGA 960
GGCATGCCCT AATTTCACCC ACAAATGCTA CTAAGCCCAG GCCCTTATCC AGCCAAAACC 1020
ATCCTGCCAA GCTCCCACCA CCACCATCAG CATCATTTTC AGGTTGTTGG TCATCACTGG 1080
TTGTTGGTCA TCACTGGTTG TTGGTCATCT ATGTCACCTA ACAGGCCACT CATGACGTTA 1140
GCCCTTGACT TCAAAAAGGA CCTCAAAGAA AATTCCAGTT TTCACTCCAA AAGGAGAAAT 1200
CAGGCCGAGC TGTGATGGCT CATGCCTGTA TTCCCAGCAC TATGGGAGGC TGAGGCAGGC 1260
GGATCGCTTG AGCCCAGGAG TTTGAGACCA CCCTGGGCAA ACCTATCTTT CCAAAAAAAT 1320
ACAAAAAGAT TAGCTGGGCA TGGTGGTGCG TGCCTGTAGT CTCAGCTAGT CAGGAGGCTG 1380
AGGTGGGAGG ATCACTTAAG CCTGGAAGGT TGAGGCTGCA GTGAGCGGTG ATGGTGCCAC 1440
TGCACTCCAG CCTGGATAAC AGAGCAAGAT GCTGTCTCAA AAACTAGCAA ACGAAACAAA 1500
AGGAGAAACT GCTGGCAGCC CCTAATCTAG TACTGTCCCG GCTCCACCCA CCTTCAGATC 1560
CAGCCTCCTC CCCTGGCACA CGGGAGCCCC CTCCTCTGAC TGTGCTGAAA GTGAGGGAAG 1620
ATCCCCTCTG GGGAGAGAGC TGTAGCCTTG ACCTCTGCAC ACCTTACTTA TCCAGAGCAC 1680
GAGGCAGGGC CGCTGACTCA TCCTGGTTTA CCCTGGGCTT TCCCAGTTTC AGCACTGAAA 1740
GTCCCGCATC TGGAAAAGCC CCTGAGTCGC TGACAAACCA GACAGTCCGG ACCATGCAAA 1800
GCACAGTGCA TGGTGCTTTA GCCACAAAGT TGATTGAAAA GTCAGAGGCA GTGAGCCACA 1860
GGAAGCGCCA CGTGACCCAG ACTGCGAGGA GGACACAGGA AACCAACCCT CACTGTGTCC 1920
TGCTAGGGGG TTAACCCGTC TACAAGCATC AGGGTTGCCA TTTCAGAGAT CAGCAAACTG 1980
AACAGCAGTC GTGACTTGTC CTCGCCTGCA AGACAAGCGA GTAACAAATC CATGAAGGGA 2040
AGGACACGGA ATTGAGCAAG GGGGCAGGGC CGGATGTCAT TTTGGCGTTT TTTTTTCTTT 2100
CAGTGATTGA GGTAAAATTC ACATAACATA AATTAACCAT TTTAAAGTGT ACGATTCAGA 2160
GGCATTTGGT ACATTCACAC TGTTGTGCAA GCACCACCTG TATCTCGTTC CAAAATATTT 2220
TCACTTCCCC AAAAGGAAAC TGTGTCCCCA TCAAGCAGCC ACACCCTACT CCCTCACCCC 2280
CGCCCCCAGC CTCTGACAAC CACCAATGTA CCTTTTGTCT CTATGGATTT GCCTTTACTG 2340
AACAATTCAT AGTAATGGAA CCATACAATA TGTAGTCCTT TGCGACTGGC TTTTTTTACT 2400
CAGCATCAAT TTTTTTTTCT TTTTCTTCGA GACAGAGTCT TGCTCTGTCA CCCCGGCTGG 2460
AGTGCAGTGG CATGATCTCG GCTCACTGCA ACCTCCACCT CCTGGGCTCA AGCGATTCAC 2520
ATGCTTCAGC CTTCTGAGTA GCTGGGACTG CAGGTGTGCA CCACCATGCA TGGCTAAATT 2580
TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT TTTTTTTTAG AGAGGGAGGT CTTACTACAT 2640
TGCCCAGACT GGTCTCAAAC TCCTGGCCTC AAGCAATCCT CCTTCCTCGG CTTCTCAAAG 2700
TGCTGGGATT ACAGGCTTGA GCCATCACGC CCAGCCTATC ATCCTAGTTT TGTTTTTTGG 2760
GTTTTTTGTT TGTTGGTTGG TTTGTTTGTT TGTTTTTGAG ACCTAGTTTC ACTCTTGTCA 2820
CCCAGGCTGG 2830