EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS187-13496 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr2:85171540-85174280 
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: 19             
IDCoordinateTissue/cell
SE_10467chr2:85171905-85172730CD19_Primary
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_25084chr2:85172188-85172641Colon_Crypt_3
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
GGTGCCTGGT GGCTGGGGGT CCCCGACATA GCTTGAGGAT GGGGGCTGGT CACCAGAGAG 60
ACCAAGGCAT GACAGAATTG GAACTTTCAG CTCATCCCCA GACCTCCAGG AAGGAAAAGG 120
GGCTGGTGAT TGAGTCAATC AGCATTGGTC AATGATTTCA TCAATTGTGC CTGTGTAATG 180
AAACCTCCAT AAAAACCCCT AAATGATGAG ATTCGGGGAG CTTCCAGTTG GTGAACACAC 240
TGAAGTGCTA GGAGGGCGGC CTGCCAGAGG AGACATAGAA GCCCTGCGTG CCCCTCCAAT 300
ACCATGCCCT ATGCTTCCAC CTGGCTGTCT CTGAGCATAT GTCCTTGATC ATAAAGTGGT 360
AAGCCTAACG AAAGTGTTTC CGAGTTCTGT GAGCCATTCT GGCAAATTAT TGAACATGAA 420
GAGGGGGTTG TGGTAACCTA GGACTTCTAT AGCTGGTTGG TTAGAAATAC AGATGGTAAC 480
CTGGTACCAG CAACCGACAT CTGAAATCAG GGCAGTCTTG CGGGATGGAG CTCTTTGGTG 540
GCATTGACAC TAATTCTAGG TAGATAATGT CAGAATGGAA TTGATTTGTT GGATACCCAA 600
TTGGTATCTG GAGAGTTGAA TAACTGGTCA GTATAAGAAA AAACTCACAC ATTTGGTGGC 660
AGAAGTATTG TGAATAAAAA CAGTTCAGAG CTCCCCTACT CCCAAACCAG AAAACCTGGA 720
GTCATCTTCG ATGCCACCCT CTCACCACCC ACCCTCTGCA CTATCCCTGC CAATCACTTG 780
CCAAGTTACC CTGATTCCAC CTCCAAATAC CTCTCTCATC TCCCGTCTTC ACTTTTCATT 840
CATCATTTAC TCATTCAATC ACAAATATTT GCTCTTATCT TCTCTGTGCC AGGCTTTGTG 900
ATAGGCATTG GAGTCAGAAG AATGAATGAG ACCTGGTAGG AAAATCACAA TCTAGTGGTA 960
AAACAAAAAC CAGAACACAA TCATAAAGCA ATGGGATTCA CACTCAGAAA TGCATAGAGC 1020
TGCTGGGCGT GGTGGCTCAT GCCTGTAATC CCATCACTTT GGGAGGCCGA GGTGGGCGGA 1080
TCATGAGGTC AGGGGTTCGA GACCAGCCTG ACCAACATGG TGAAACCCTG TCTCTACTAA 1140
AAATACAAAA TTAGCTGGGC GTGGTGGCAC ATGCCTGTAA TCCTGGCTAC TCAGGAGGCT 1200
AAAGCAGGAG AATCACTTGA ACCTGGGAGG CAGAGATTGC AGCAAGCCGA GATCGCACTA 1260
CTGCACTCCA GCTTGGATGA CACAGTGAGA CTCTGTCTCA AAAAAAAAAA AAAAAAAAAG 1320
AAAAGAAAAG AAAAGAAATG CACAGAGCAT CATAGAGTCC AGGGCAGGGG TCCCTGACCA 1380
AGCTCGGGAA TGGTGGGGGA TGGGGTGGGG ACATCAGTGG AGTTTTTTGG GGTTTTTTGT 1440
TTTGCTTTGT TTGAGACAGG GTCTTGCTCC GTCACCCAGG CTGGAGTGCA GTGGTGTGAT 1500
CATAGTTCAC TGCAACCTTG AACTCCTGGG CTCAAGGGAT CCCCCGGCCT CAGCCTCCTG 1560
AGTAGCTGGG ATTACAGGCA TGAGCCACCA CACCCAGTCA ATAGACTTTT CTTGATGTGG 1620
GTGACACCCA AGCTTTAAGT TTGAAGACTA AAGGAGAGCT GGCACACCAA CAGTATACGA 1680
GGGGAGGGGA GGGGAGAGGG GAGGGGAGAG GAGGGGAGAG GGGAGGTGAG AGGGGAAGGG 1740
AGGGGAGGGA GGAGGGGAGG GGAGGGGAGG GGAGAGGACA CAGCAGGCTG GTAGGGCAGC 1800
TTTGAATATG GCTCAGAGGC GAGGCGAGCA AGGTCTGAAT CACTTCTGCT CCAAGTCCAG 1860
GCCCACATTA CTTCTTATAC GGACAAGAGG CCAGTAACTG CTCTACCCAC ACATTCTCCT 1920
CCCCTACCAT CAGAAAAATC TCCCTAAAGC TCAAATTTGA CTTCCTGTCT CCCCTGCTTG 1980
CTACCCTCTG CTGGTTCCCC TTTCTGATCT GTGGTGTCTC AGCTCCACCT CTGTTCATAA 2040
ACTTCATATG GTGCCTTCAA AAGTATTTCC GTCTCTGGAC CTTCATCCCT GCACTACTGT 2100
CTGCCTGGAA TTTCCTGCCC TGCCTTGGTT GATGAGGTGG ACTCCTATTC ATACTTCAGA 2160
GTGACTCAGA TGTGACTTGT TCCACAAAGT CCCCACCCAC TTGCACTCAC CTCCGTGGTG 2220
CACGTATTCC AGGGCCGTGA GCTTCACCTC TCTGCACGTC TCCCTCCTGC TACAGCTGTG 2280
AGGGTGCAGA CCTCCTCTGC TGGCACCAGG GCCCGGCCTG CAGTGGGCCT TTGGCAAATG 2340
AGGAACTAGG GCTACCGGTA GGTGAAAATG CAGCTAATGC CCAGGAAGCT AGAAGCTGTT 2400
GGAACATTTC TGAGACCCTT TAGACCTGGA AATAGCTCTA TGTTAGAGGG TTGCTGATAG 2460
AGAAGGCTGG AAGTGAGGTC CCTCTGTCCC CAGCTCGCCT CAGACCCTGG TTCCAGATAC 2520
AGTTGCATGT GTTTCCAACC AAGACTCTGA CCTGGCTCCT CAACCAAACC TCCCCTGCGT 2580
CCATGGATCT ATCTGAACTC CCATTTATAA TCGTAAGAGG CTGTGGGTTA GAGGCGCTGT 2640
GCTAATGATG GCTGTATGGT TATTATGATT GTGAAGTTGT TATATTTTAC ATAGAATACA 2700
AGTTTATGTA CATTACGATT AAGACTAGTA AAGCTCTTTG 2740