EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-37241 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr2:85172860-85174320 
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
AAAAGAAAAG AAAAGAAATG CACAGAGCAT CATAGAGTCC AGGGCAGGGG TCCCTGACCA 60
AGCTCGGGAA TGGTGGGGGA TGGGGTGGGG ACATCAGTGG AGTTTTTTGG GGTTTTTTGT 120
TTTGCTTTGT TTGAGACAGG GTCTTGCTCC GTCACCCAGG CTGGAGTGCA GTGGTGTGAT 180
CATAGTTCAC TGCAACCTTG AACTCCTGGG CTCAAGGGAT CCCCCGGCCT CAGCCTCCTG 240
AGTAGCTGGG ATTACAGGCA TGAGCCACCA CACCCAGTCA ATAGACTTTT CTTGATGTGG 300
GTGACACCCA AGCTTTAAGT TTGAAGACTA AAGGAGAGCT GGCACACCAA CAGTATACGA 360
GGGGAGGGGA GGGGAGAGGG GAGGGGAGAG GAGGGGAGAG GGGAGGTGAG AGGGGAAGGG 420
AGGGGAGGGA GGAGGGGAGG GGAGGGGAGG GGAGAGGACA CAGCAGGCTG GTAGGGCAGC 480
TTTGAATATG GCTCAGAGGC GAGGCGAGCA AGGTCTGAAT CACTTCTGCT CCAAGTCCAG 540
GCCCACATTA CTTCTTATAC GGACAAGAGG CCAGTAACTG CTCTACCCAC ACATTCTCCT 600
CCCCTACCAT CAGAAAAATC TCCCTAAAGC TCAAATTTGA CTTCCTGTCT CCCCTGCTTG 660
CTACCCTCTG CTGGTTCCCC TTTCTGATCT GTGGTGTCTC AGCTCCACCT CTGTTCATAA 720
ACTTCATATG GTGCCTTCAA AAGTATTTCC GTCTCTGGAC CTTCATCCCT GCACTACTGT 780
CTGCCTGGAA TTTCCTGCCC TGCCTTGGTT GATGAGGTGG ACTCCTATTC ATACTTCAGA 840
GTGACTCAGA TGTGACTTGT TCCACAAAGT CCCCACCCAC TTGCACTCAC CTCCGTGGTG 900
CACGTATTCC AGGGCCGTGA GCTTCACCTC TCTGCACGTC TCCCTCCTGC TACAGCTGTG 960
AGGGTGCAGA CCTCCTCTGC TGGCACCAGG GCCCGGCCTG CAGTGGGCCT TTGGCAAATG 1020
AGGAACTAGG GCTACCGGTA GGTGAAAATG CAGCTAATGC CCAGGAAGCT AGAAGCTGTT 1080
GGAACATTTC TGAGACCCTT TAGACCTGGA AATAGCTCTA TGTTAGAGGG TTGCTGATAG 1140
AGAAGGCTGG AAGTGAGGTC CCTCTGTCCC CAGCTCGCCT CAGACCCTGG TTCCAGATAC 1200
AGTTGCATGT GTTTCCAACC AAGACTCTGA CCTGGCTCCT CAACCAAACC TCCCCTGCGT 1260
CCATGGATCT ATCTGAACTC CCATTTATAA TCGTAAGAGG CTGTGGGTTA GAGGCGCTGT 1320
GCTAATGATG GCTGTATGGT TATTATGATT GTGAAGTTGT TATATTTTAC ATAGAATACA 1380
AGTTTATGTA CATTACGATT AAGACTAGTA AAGCTCTTTG GAACTTTAAA AACAAATCCC 1440
AGTCAGGCGT GATGGCTCAC 1460