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

TagContent
EnhancerAtlas ID
HS110-02742 
Organism
Homo sapiens 
Tissue/cell
KATO3 
Coordinate
chr2:85172870-85174520 
TF binding sites/motifs
Number: 18             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr2:85173278-85173296GGAGGGGAGGGAGGAGGG+6.27
RREB1MA0073.1chr2:85172930-85172950TGGTGGGGGATGGGGTGGGG-6.83
ZNF263MA0528.1chr2:85173261-85173282GGAGGTGAGAGGGGAAGGGAG+6.02
ZNF263MA0528.1chr2:85173231-85173252GGGAGAGGGGAGGGGAGAGGA+6.15
ZNF263MA0528.1chr2:85173229-85173250AGGGGAGAGGGGAGGGGAGAG+6.19
ZNF263MA0528.1chr2:85173243-85173264GGGAGAGGAGGGGAGAGGGGA+6.33
ZNF263MA0528.1chr2:85173236-85173257AGGGGAGGGGAGAGGAGGGGA+6.51
ZNF263MA0528.1chr2:85173246-85173267AGAGGAGGGGAGAGGGGAGGT+6.83
ZNF263MA0528.1chr2:85173292-85173313AGGGGAGGGGAGGGGAGGGGA+6.91
ZNF263MA0528.1chr2:85173241-85173262AGGGGAGAGGAGGGGAGAGGG+6
ZNF263MA0528.1chr2:85173219-85173240AGGGGAGGGGAGGGGAGAGGG+7.01
ZNF263MA0528.1chr2:85173224-85173245AGGGGAGGGGAGAGGGGAGGG+7.1
ZNF263MA0528.1chr2:85173297-85173318AGGGGAGGGGAGGGGAGAGGA+7.1
ZNF263MA0528.1chr2:85173271-85173292GGGGAAGGGAGGGGAGGGAGG+7.23
ZNF263MA0528.1chr2:85173275-85173296AAGGGAGGGGAGGGAGGAGGG+7.34
ZNF263MA0528.1chr2:85173280-85173301AGGGGAGGGAGGAGGGGAGGG+7.56
ZNF263MA0528.1chr2:85173284-85173305GAGGGAGGAGGGGAGGGGAGG+7.86
ZNF263MA0528.1chr2:85173287-85173308GGAGGAGGGGAGGGGAGGGGA+8.75
Number of super-enhancer constituents: 17             
IDCoordinateTissue/cell
SE_10467chr2:85172755-85174410CD19_Primary
SE_14858chr2:85173160-85174371CD4_Memory_Primary_7pool
SE_17329chr2:85172940-85174409CD4p_CD25-_CD45RAp_Naive
SE_18307chr2:85171711-85174762CD4p_CD25-_Il17-_PMAstim_Th
SE_19290chr2:85172506-85174415CD4p_CD25-_Il17p_PMAstim_Th17
SE_24195chr2:85173090-85174241Colon_Crypt_2
SE_25084chr2:85173093-85174407Colon_Crypt_3
SE_27502chr2:85172693-85174600Esophagus
SE_32545chr2:85164283-85174534GM12878
SE_34685chr2:85171658-85174793HeLa
SE_35873chr2:85172149-85175081HMEC
SE_47378chr2:85172889-85174696Panc1
SE_50337chr2:85171737-85174482Sigmoid_Colon
SE_52528chr2:85172218-85174434Small_Intestine
SE_54030chr2:85173005-85174218Spleen
SE_59563chr2:85151112-85174538Ly3
SE_64856chr2:85172724-85174623NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr28517332185174019
chr28517318885173797
Number: 1             
IDChromosomeStartEnd
GH02I084944chr28517148285174859
Enhancer Sequence
AAAAGAAATG CACAGAGCAT CATAGAGTCC AGGGCAGGGG TCCCTGACCA AGCTCGGGAA 60
TGGTGGGGGA TGGGGTGGGG ACATCAGTGG AGTTTTTTGG GGTTTTTTGT TTTGCTTTGT 120
TTGAGACAGG GTCTTGCTCC GTCACCCAGG CTGGAGTGCA GTGGTGTGAT CATAGTTCAC 180
TGCAACCTTG AACTCCTGGG CTCAAGGGAT CCCCCGGCCT CAGCCTCCTG AGTAGCTGGG 240
ATTACAGGCA TGAGCCACCA CACCCAGTCA ATAGACTTTT CTTGATGTGG GTGACACCCA 300
AGCTTTAAGT TTGAAGACTA AAGGAGAGCT GGCACACCAA CAGTATACGA GGGGAGGGGA 360
GGGGAGAGGG GAGGGGAGAG GAGGGGAGAG GGGAGGTGAG AGGGGAAGGG AGGGGAGGGA 420
GGAGGGGAGG GGAGGGGAGG GGAGAGGACA CAGCAGGCTG GTAGGGCAGC TTTGAATATG 480
GCTCAGAGGC GAGGCGAGCA AGGTCTGAAT CACTTCTGCT CCAAGTCCAG GCCCACATTA 540
CTTCTTATAC GGACAAGAGG CCAGTAACTG CTCTACCCAC ACATTCTCCT CCCCTACCAT 600
CAGAAAAATC TCCCTAAAGC TCAAATTTGA CTTCCTGTCT CCCCTGCTTG CTACCCTCTG 660
CTGGTTCCCC TTTCTGATCT GTGGTGTCTC AGCTCCACCT CTGTTCATAA ACTTCATATG 720
GTGCCTTCAA AAGTATTTCC GTCTCTGGAC CTTCATCCCT GCACTACTGT CTGCCTGGAA 780
TTTCCTGCCC TGCCTTGGTT GATGAGGTGG ACTCCTATTC ATACTTCAGA GTGACTCAGA 840
TGTGACTTGT TCCACAAAGT CCCCACCCAC TTGCACTCAC CTCCGTGGTG CACGTATTCC 900
AGGGCCGTGA GCTTCACCTC TCTGCACGTC TCCCTCCTGC TACAGCTGTG AGGGTGCAGA 960
CCTCCTCTGC TGGCACCAGG GCCCGGCCTG CAGTGGGCCT TTGGCAAATG AGGAACTAGG 1020
GCTACCGGTA GGTGAAAATG CAGCTAATGC CCAGGAAGCT AGAAGCTGTT GGAACATTTC 1080
TGAGACCCTT TAGACCTGGA AATAGCTCTA TGTTAGAGGG TTGCTGATAG AGAAGGCTGG 1140
AAGTGAGGTC CCTCTGTCCC CAGCTCGCCT CAGACCCTGG TTCCAGATAC AGTTGCATGT 1200
GTTTCCAACC AAGACTCTGA CCTGGCTCCT CAACCAAACC TCCCCTGCGT CCATGGATCT 1260
ATCTGAACTC CCATTTATAA TCGTAAGAGG CTGTGGGTTA GAGGCGCTGT GCTAATGATG 1320
GCTGTATGGT TATTATGATT GTGAAGTTGT TATATTTTAC ATAGAATACA AGTTTATGTA 1380
CATTACGATT AAGACTAGTA AAGCTCTTTG GAACTTTAAA AACAAATCCC AGTCAGGCGT 1440
GATGGCTCAC GCCTGTAATC CTAGCTCTTT GGGAGTCCAA GGCAGGAGGA CTGGTTAAGC 1500
CCAATTCTCC AGGAGTTTGA GACCAGCCTG GGCAACATAG TAGGACCCCA TCTCTACAAA 1560
AAAATAAAAA TCAAAAAATT AGCCAGACGT GGTGGCATGC ACCTTTAGTC CCAGCTACTC 1620
GGGAGGCTGA GGCAGGAGGA CTGTTTGAGC 1650