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

TagContent
EnhancerAtlas ID
HS105-15210 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr11:75057430-75060060 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
PRDM1MA0508.2chr11:75060016-75060026TCACTTTCAC+6.02
RESTMA0138.2chr11:75057783-75057804GGTGCTCTCCAAGGCCCTGGC-6.39
TFAP2AMA0003.3chr11:75058186-75058197AGCCTCAGGCA+6.32
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00135chr11:75043906-75064147Adipose_Nuclei
SE_03287chr11:75057659-75058257Brain_Angular_Gyrus
SE_03287chr11:75058541-75059658Brain_Angular_Gyrus
SE_04031chr11:75054968-75063972Brain_Anterior_Caudate
SE_04951chr11:75048891-75064200Brain_Cingulate_Gyrus
SE_05927chr11:75046856-75064439Brain_Hippocampus_Middle
SE_07122chr11:75047688-75064272Brain_Hippocampus_Middle_150
SE_07907chr11:75048701-75062762Brain_Inferior_Temporal_Lobe
SE_09621chr11:75043963-75064807CD14
SE_13044chr11:75057421-75058564CD34_Primary_RO01480
SE_13386chr11:75055626-75064677CD34_Primary_RO01536
SE_14290chr11:75057685-75058539CD34_Primary_RO01549
SE_23271chr11:75056917-75058479Colon_Crypt_1
SE_24003chr11:75057241-75057718Colon_Crypt_2
SE_24003chr11:75057837-75058409Colon_Crypt_2
SE_25192chr11:75057799-75058411Colon_Crypt_3
SE_25898chr11:75044092-75062820Duodenum_Smooth_Muscle
SE_26962chr11:75055050-75064351Esophagus
SE_28109chr11:75058258-75059776Fetal_Intestine
SE_29208chr11:75058066-75059586Fetal_Intestine_Large
SE_29208chr11:75059784-75064536Fetal_Intestine_Large
SE_31429chr11:75055051-75059711Gastric
SE_41608chr11:75055060-75058428LNCaP
SE_41608chr11:75058868-75059479LNCaP
SE_42220chr11:75048188-75064405Lung
SE_46889chr11:75058176-75059523Ovary
SE_47208chr11:75043719-75064671Panc1
SE_49380chr11:75056853-75059854Right_Atrium
SE_49998chr11:75055087-75059597RPMI-8402
SE_49998chr11:75059752-75062703RPMI-8402
SE_50175chr11:75055026-75064419Sigmoid_Colon
SE_52494chr11:75055037-75059806Small_Intestine
SE_53599chr11:75048063-75059815Spleen
SE_54712chr11:75043970-75064153Stomach_Smooth_Muscle
SE_59773chr11:75038940-75077709Ly4
SE_65484chr11:75054477-75058471Pancreatic_islets
SE_65484chr11:75058612-75063754Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr117505787475059565
Enhancer Sequence
GGCAGAGGGA GGGGGTGGAT GAGATAAAAC CCCTAGGTTC CCATACCCAG TCTTCACTGC 60
CTGCCGCCAT ACTGCTTGCT CCCAGCCCAG GGCCTCACGC CCTTCCTCCA AGAGGCTCAA 120
GCCTTGCTCC AGGCATGTAG AAAAGCAGGG TCCCCTCCCA CTCCTCTCTG CCCGCTGTAG 180
CCTAGTTTTG CCCTCACCAC TCCACCAAAA CCCATGCCAC CAGCTAATGC CTTCTGGCTG 240
AATCTGAGGG GTCTCGCTCC AGCTCATCCT CTGTGGGTCT GTCCCTGCTT CTTTGGCTCC 300
AAGAATATGG CCTTCCGTCA GTTTCCTCCC TCTTCTCTCC ATACCCAGGC ACTGGTGCTC 360
TCCAAGGCCC TGGCTGTCCC TAATCATCCT CTCTTCATAC TCTATACCTC CTCCCTATGC 420
GATGTCATTC ATCCACATTT CCAAAGCCCT GCCTCGCACC TTGATTCTTA CCCCAGGATC 480
CAGACCCTTC TATGCAGAAG CCCCACTACG TCCAGCCTAT AACAGACTGC CCTGGCTCCC 540
TCACCAAGCT GCTCCCAGCC ATGCAGGCCT CAGCCAGATG GTAGGCGCGG GCACTCTGGC 600
AGTAGCGGAG CATGGCTGTG TAGAGGCCAG GACCTCACTT GGGGTGTGCT GACTCCCAGC 660
CTGCTGTTCT ACTGCCACCA ACCCAAAGTG TCAGAAGCCC TGGAAGTGGC AAGCCCACAA 720
CTCAGGACCT CTGGACCCAT GCCAACGGGA GGCGTCAGCC TCAGGCAAGG AGGCCCAAAC 780
TTGGAAGGAA GAGAGCAGTG GAGAAGTCTG AAGCCCAGAG GCCGGCCTGG AATCAGGGAT 840
CAGAGACAGT GGGCCAGACT TGATGCTACC ACTCCCAGCG GCCCCATGAG CAGCCCTGGC 900
CAAAGCCACA GGACTTCCCC ATGTTCCAGC CAAGATGGGT CACACAGGGC TTAACCACCA 960
AGAGAAATGA CAGCCAAAGT TCACAGAGAG CTGGTGATTA CATGTCCTCA TCACCCTCCT 1020
TTCTCTGAAA AAAGAGGAGT TCATCTGCAG GAAAGGAAAT TCCATTCCCT ACCACTGCCT 1080
CTCAGGAAGT CCCTCCTGTT GTCTAAATCT GATCCTTCAT GTTGTCTGTT GAGTAAGTGG 1140
AAACGGCAAG GCCCAGAAAG GACGCACAAC TTGAGGCTGG GAGCTGCTGG GGAGGCCAAC 1200
TGTGAGCCAG ACAAGGCCCC CTCTCTTGGG CAAAAGCGTC GAGTAGCAGA GAGGGCTTTG 1260
TGGGTCAATA GGCCTGGGTT CTTATGCTTG CTGGCTGAAT GGCAGTGAAC AAATACTTAA 1320
TCTCTTCTAG TCTGTTTCCT CATCTGCAAA ATGGGGACAA CAATGACTAC ACTACTAGAT 1380
TACAGTTGAA TTCATTGAGA TTATGCGTGT AATTCTAACA CACACCAGAT ACCTGGCAAA 1440
GGTCCAATCG ACCAGCAAGG TTGATGGACT CCACCTCCTA TTCACATTCA TATTTCTCAA 1500
CTCTATCCTC TCTGCAGCCT AAGTTCAGAG CTCACAGCCT TAGTTCTCAG GTTTCTCCCC 1560
AGCCTCCTCA CTGGTCTTCC TGCTTCTAGG CCTGCTCTTC CCATCCACCC TACTTGGCGC 1620
TGCCAAAGAC ATCTCTCTGA AATGAAAACA TCTGCTTCCA GCCCTCTGCT GCCTCACACT 1680
CTTCTCTGAA TCACCATCCA CTTCAGGAGA AAATGCTCTC TCCTTAGCCT GACATTCCCA 1740
GACTGCTGGT GACCGGTCTG TGTTTACCTC TTAAGGCTCA CTATCATCCC CAGCCCAGGC 1800
CCCAGGCTGC ACGCCTTGCT TCCTGCCTCC AAGCCACTGC ACATTCTGCA CCCTTGGCCA 1860
GAAATATCAT TCCCAATCCC GCCCCCTTGG CCTATTCATC CTTCCAGATG AAGCTCAGTA 1920
GTTCCAACGC CACCTCCTTT CCAGGAGAGC TTCCTGTACC ATGCTCCCTG CCTGGGCCTG 1980
GGTTGGGGAC TTCTCCTTAA GCCTCCCACA ACACATGTCA TCCTGCGTTA TGACCACCTG 2040
CTCTGCTCTA AATCCCTGGA GGACAGAGTA GACTCCTTCC TTGCTGAATC CCCAGGCCCT 2100
GGGCACTCAG AAGGCACTCA TCAACATTTG TTGAATGAAT ATATGATTGT TCCCAGAGCA 2160
CCTTGCAGCA ACCATCATAC TCCTGCCCTG TGATTAGTCC TGTCCAGGTA TTTTTTTTTT 2220
TTATTTTTTC AGACAGGGTC TCACTCTCTC ATCCAGGCTG GAGTGCAGTG GCATGATCAT 2280
GGCTCACTGC AGCCTTAACC TCCAGGGCTC AAGTGATCCT CCCACTTCAG CCTCCAGAGT 2340
AGTTAGGACT ATAGGCATGT GCCACCACAC TCAGCTAATT TTTGTGTTTT TTGTAGAGAT 2400
GGTATGTTGC CCAGACTGGT CTCGAACTCC TGAGCTCAAG CAATCTGCCC ATCTCAGCCT 2460
TCCAAAGTTC TAGGATTACA GGCGTGAACC ACCGCGCACA GCCCTGTCCA GGTATTTAAC 2520
ACCTCTTTCC CCCTTGACCC TGGGAGTTCC TAGAGGGCAA TGACAGTTTG TGATAAATTT 2580
TCATTGTCAC TTTCACATGG GGGTGCAATT CCAGATGGAG GGATGGTTGC 2630