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

TagContent
EnhancerAtlas ID
HS051-05029 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr11:75039540-75041790 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr11:75041401-75041421CCCCACCCCACCCCATAACA+6.79
RREB1MA0073.1chr11:75041411-75041431CCCCATAACACCCCACACCA+7.01
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00135chr11:75039089-75039942Adipose_Nuclei
SE_03287chr11:75038989-75039940Brain_Angular_Gyrus
SE_03287chr11:75041374-75041920Brain_Angular_Gyrus
SE_04031chr11:75038878-75040252Brain_Anterior_Caudate
SE_04031chr11:75040313-75041841Brain_Anterior_Caudate
SE_04951chr11:75038698-75042281Brain_Cingulate_Gyrus
SE_05927chr11:75039003-75042234Brain_Hippocampus_Middle
SE_07122chr11:75039139-75040925Brain_Hippocampus_Middle_150
SE_07907chr11:75038776-75042175Brain_Inferior_Temporal_Lobe
SE_09621chr11:75038907-75042083CD14
SE_13044chr11:75039978-75040895CD34_Primary_RO01480
SE_13044chr11:75040931-75042114CD34_Primary_RO01480
SE_13386chr11:75038965-75042257CD34_Primary_RO01536
SE_14290chr11:75039890-75042323CD34_Primary_RO01549
SE_23271chr11:75039239-75042140Colon_Crypt_1
SE_24003chr11:75039434-75040136Colon_Crypt_2
SE_24003chr11:75040325-75040915Colon_Crypt_2
SE_24003chr11:75041047-75041451Colon_Crypt_2
SE_25192chr11:75039037-75042197Colon_Crypt_3
SE_25898chr11:75038978-75042365Duodenum_Smooth_Muscle
SE_26962chr11:75039418-75040908Esophagus
SE_26962chr11:75041074-75042209Esophagus
SE_28109chr11:75039189-75042419Fetal_Intestine
SE_29208chr11:75039169-75042452Fetal_Intestine_Large
SE_31429chr11:75039234-75042571Gastric
SE_41608chr11:75039364-75040307LNCaP
SE_41608chr11:75040350-75040855LNCaP
SE_41608chr11:75041068-75041957LNCaP
SE_42220chr11:75039229-75042237Lung
SE_47208chr11:75032345-75042889Panc1
SE_49998chr11:75038987-75042142RPMI-8402
SE_50175chr11:75039169-75042236Sigmoid_Colon
SE_52494chr11:75039154-75042185Small_Intestine
SE_53599chr11:75039370-75040854Spleen
SE_54712chr11:75038901-75042420Stomach_Smooth_Muscle
SE_59773chr11:75038940-75077709Ly4
SE_65484chr11:75039192-75040460Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr117504122775041400
chr117504140075041600
chr117504136175041638
Enhancer Sequence
ATGGTGACTT GAACTGAAGC CCCTGCCGCC CAAATGAAAG TGCCCTTCTT ACATCCTTGT 60
CTCCCACCAG CCATTCACCC ATCCCAAGTG TCATGCCTTC CCTGGGCATC TGTTACCACA 120
TTCTGGGCTC TGTGCCAACT GCTGGCCACC TGGTGTGGAC AGCTCAGGCC AAGTCCCAGA 180
CTCTACTATA GTCTGAAGCT GCAGAGGCCT GGAGGCTGCA GTCTCACCCT CTGGGATGGG 240
CTCCTGTCCA GCCAAGGAGT CCCAGGATCC AGGGCCAGGG GCCAGGCATA CCACATCCAA 300
GATGCGTATA GACAGGAGTG CCCTGCTCCT GCCCTCCCTG GATCCCAGTA TTCCTCAATG 360
CACAGAGGAA GATGGCCCCC AGCAGATGGC TCCAGAGATC TGCACAGCAA AACCATTGAG 420
TGGAACGGGA ACGGCTGGGC TGAGAGGGCC GTCAGAAAAC ACTGAACTCA GAGCCCTGAA 480
GAGAGTGGGG CAGCCAGTAA GGGTTTCCCA TGCAAATTGG TCACTGCACC TCTCAAATGT 540
AAACACACTA GAAACAGCAC TTCGCTGGGA CCATTCCTTC CTGCTGTGTA ACTTTTTTTT 600
TTTTTTTTTT TTTTTGAGAC AAGTTCTTGC TCTGTCACCC AGGCTGACAT GCAGTAACAA 660
TTACGGCTCA CAGGGCTCAC TGCAGCCTCA ACATCCTGTG TTCAACTGAT CCTCCCACCT 720
CAGCCGCCTG AGTAGCTGGA ACTATAGGCA CGCACCACCA TGTCTAGCTA ATTTTTTGTA 780
TTTTTTATAG AGATGGAGGG TCTCACCATG TTGCTCAGGC TGGCCTGGAA CTCCTGGGCT 840
CAAGTGATCC TCCTGCCTTG GCCTCCCAAA GTGCTGGAAT TACAGGTGTG AGCCACTGAA 900
CCTTGCTGCT GTGTAACCTT GAGCCAAACC TTCTCTGAGC CATCTCTGCC TAAAAGCAGG 960
GTTCAGGGAT CTAGAATTCC AGATTCTAGG GTGGGAGGAG TGGGTTGTCC TTGCAGAGCC 1020
CCTCCTGTTA AAGACTACAT CCACTCAAGC TGTCTCTTTG TGTAAGATGG TGTGACTATG 1080
ACCACTACGC GGACCACTGC CTTCCTGGCC TTTCACGAAA CCACCTTCTG CCACACATTA 1140
GCCTGTTAAT GGGACCATCC TCAGAGGGTT TCTGACATTC CATGTGGGGA CGAACAGTCA 1200
CAATAATCAC TACTGGCTGG GCACTGTGGT GCATGCCTGT AATCCCAGTG CTTTGGGAGA 1260
TCAAGGTGGG AGGATTGCTT GAGCCCAAGA GTTTGAGACC AGCCTGGGCA ACATAGTAAG 1320
ACTCCATCTC TACAAAAAAT TTTAAAATCT ACCCAGGCAT GGTAGCACAT ACCTGTGCTA 1380
CAAGTCTCAG CTACTTGAAA AGCTGATGCA GGAGGATCAC TTGACCCCAG GAGTTCGAGG 1440
CTGCAGTGAG ATGTGATTGC ACCACTGCAC TCTAGCCTGA ATGACAAGAC TGAGACCCTG 1500
TCTCTAAAAA AAAAAAAAGT CACTACTGCC TCTCAGACTC CCTTTCACAC ATGACAGAGG 1560
CCTGACAAAT TTGCACTGAA TGAATAAATG AACGAACGAA CAATCTGTCA CTCATTTCCC 1620
AACTTCTAGC CTCTCTCTTC TAGTCTATTT ACCTACACAG CTGCCACGTG AACCTTCAGA 1680
TCCTGCTGCT CCTGCAAGCT GTGTGTTCAG ACAAATTGCT GAACTTAGCT GAGCCTTCAA 1740
TTCCTCAACT ACAAACAGGG ACTCTACTTG GGTAATTAGG AAGATTGAAA GAAAGCATAA 1800
GCACAGCATC TCAAGGGCTA AGGAGGAGTC CAGGAAAAGC TGTTGAAGGA AAGCTGTTTC 1860
TCCCCACCCC ACCCCATAAC ACCCCACACC ACCCTGATCC TCTAATCTCT CTGTTCCAAA 1920
GGCTGCAGGA AAGAGCCCAG CCCCTGGGCT GGCCCCTGGC TATATGTAAA TGTTTATGCC 1980
AAGCCCAGCC TCCTAAGGAC AAGTTATTTG CTTTGCTTGT AATTAATTGC AGAAGGCCTG 2040
CCTGGGTAAT AAACTCTGCC GAAGAAATAT AAACAGTTTG CACAGAGCTT CAAATCCATT 2100
GTGAGGCCAA GAGAAAGGGT CTGCTAGGAA TGGAATGTTC TCCCCAGTCT TCCTCTAAGC 2160
TGGAGGCAGA GAGATCACTG AAGGTCAGAA CTGAGAGGAC CCTTGGAAAT CATTTGAAAA 2220
ATAGCACCTG GCATCATGAC CTTGTTCCAG 2250