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

TagContent
EnhancerAtlas ID
HS187-04695 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr11:75039010-75041640 
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
ACATAAAGTG AACAATTCAG TGGCATTTAG TCCATTCACA ACGTTGTGCA AAACCGCCAC 60
TTCTATCTAG ATCCAACGCA TTTCCATCAC TCCAAAGTAA AACCCCTTAC TCACTATGTA 120
GTCTCTCCCC ATTCTTTCCT CTCTCCAACC CCTGGCAACT ACCAGTGTCT GCTTTCTGTC 180
TCTATGGATT TCTCTATTCT GGATATTTCA TACAAGTTGA CTCATACTAT AGGTGACCTC 240
TTGTGTCTGG CTTTTTTCAT TTCACGTAAG GTTTGCAAGG TTCGTCCACT TTATAGCATG 300
GATCAGTATT TCATTCCTTC TCATGGGTGA ATAATGTTGT ACAGCATGGA TATACCACCA 360
TTTGTTTATC CATTCATCTG CAGATGGGCA TTTAGGCTGT CTGTTCCCAC TTTTTGGCTA 420
TTGTGAATAG TCAGTTGCTG CCTGTTCCTC CTCCCTAAAA CCCTGTGAAT GAGGACAGTT 480
GTTCATCCCC ATTCCCCAGA AGACAACATT GAGGTTCATT TGTGATACAG ATGGTGACTT 540
GAACTGAAGC CCCTGCCGCC CAAATGAAAG TGCCCTTCTT ACATCCTTGT CTCCCACCAG 600
CCATTCACCC ATCCCAAGTG TCATGCCTTC CCTGGGCATC TGTTACCACA TTCTGGGCTC 660
TGTGCCAACT GCTGGCCACC TGGTGTGGAC AGCTCAGGCC AAGTCCCAGA CTCTACTATA 720
GTCTGAAGCT GCAGAGGCCT GGAGGCTGCA GTCTCACCCT CTGGGATGGG CTCCTGTCCA 780
GCCAAGGAGT CCCAGGATCC AGGGCCAGGG GCCAGGCATA CCACATCCAA GATGCGTATA 840
GACAGGAGTG CCCTGCTCCT GCCCTCCCTG GATCCCAGTA TTCCTCAATG CACAGAGGAA 900
GATGGCCCCC AGCAGATGGC TCCAGAGATC TGCACAGCAA AACCATTGAG TGGAACGGGA 960
ACGGCTGGGC TGAGAGGGCC GTCAGAAAAC ACTGAACTCA GAGCCCTGAA GAGAGTGGGG 1020
CAGCCAGTAA GGGTTTCCCA TGCAAATTGG TCACTGCACC TCTCAAATGT AAACACACTA 1080
GAAACAGCAC TTCGCTGGGA CCATTCCTTC CTGCTGTGTA ACTTTTTTTT TTTTTTTTTT 1140
TTTTTGAGAC AAGTTCTTGC TCTGTCACCC AGGCTGACAT GCAGTAACAA TTACGGCTCA 1200
CAGGGCTCAC TGCAGCCTCA ACATCCTGTG TTCAACTGAT CCTCCCACCT CAGCCGCCTG 1260
AGTAGCTGGA ACTATAGGCA CGCACCACCA TGTCTAGCTA ATTTTTTGTA TTTTTTATAG 1320
AGATGGAGGG TCTCACCATG TTGCTCAGGC TGGCCTGGAA CTCCTGGGCT CAAGTGATCC 1380
TCCTGCCTTG GCCTCCCAAA GTGCTGGAAT TACAGGTGTG AGCCACTGAA CCTTGCTGCT 1440
GTGTAACCTT GAGCCAAACC TTCTCTGAGC CATCTCTGCC TAAAAGCAGG GTTCAGGGAT 1500
CTAGAATTCC AGATTCTAGG GTGGGAGGAG TGGGTTGTCC TTGCAGAGCC CCTCCTGTTA 1560
AAGACTACAT CCACTCAAGC TGTCTCTTTG TGTAAGATGG TGTGACTATG ACCACTACGC 1620
GGACCACTGC CTTCCTGGCC TTTCACGAAA CCACCTTCTG CCACACATTA GCCTGTTAAT 1680
GGGACCATCC TCAGAGGGTT TCTGACATTC CATGTGGGGA CGAACAGTCA CAATAATCAC 1740
TACTGGCTGG GCACTGTGGT GCATGCCTGT AATCCCAGTG CTTTGGGAGA TCAAGGTGGG 1800
AGGATTGCTT GAGCCCAAGA GTTTGAGACC AGCCTGGGCA ACATAGTAAG ACTCCATCTC 1860
TACAAAAAAT TTTAAAATCT ACCCAGGCAT GGTAGCACAT ACCTGTGCTA CAAGTCTCAG 1920
CTACTTGAAA AGCTGATGCA GGAGGATCAC TTGACCCCAG GAGTTCGAGG CTGCAGTGAG 1980
ATGTGATTGC ACCACTGCAC TCTAGCCTGA ATGACAAGAC TGAGACCCTG TCTCTAAAAA 2040
AAAAAAAAGT CACTACTGCC TCTCAGACTC CCTTTCACAC ATGACAGAGG CCTGACAAAT 2100
TTGCACTGAA TGAATAAATG AACGAACGAA CAATCTGTCA CTCATTTCCC AACTTCTAGC 2160
CTCTCTCTTC TAGTCTATTT ACCTACACAG CTGCCACGTG AACCTTCAGA TCCTGCTGCT 2220
CCTGCAAGCT GTGTGTTCAG ACAAATTGCT GAACTTAGCT GAGCCTTCAA TTCCTCAACT 2280
ACAAACAGGG ACTCTACTTG GGTAATTAGG AAGATTGAAA GAAAGCATAA GCACAGCATC 2340
TCAAGGGCTA AGGAGGAGTC CAGGAAAAGC TGTTGAAGGA AAGCTGTTTC TCCCCACCCC 2400
ACCCCATAAC ACCCCACACC ACCCTGATCC TCTAATCTCT CTGTTCCAAA GGCTGCAGGA 2460
AAGAGCCCAG CCCCTGGGCT GGCCCCTGGC TATATGTAAA TGTTTATGCC AAGCCCAGCC 2520
TCCTAAGGAC AAGTTATTTG CTTTGCTTGT AATTAATTGC AGAAGGCCTG CCTGGGTAAT 2580
AAACTCTGCC GAAGAAATAT AAACAGTTTG CACAGAGCTT CAAATCCATT 2630