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

TagContent
EnhancerAtlas ID
HS105-13818 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr11:44594380-44599140 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs60865046chr1144594611hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CremMA0609.1chr11:44594785-44594795TATGACGTAA+6.02
KLF4MA0039.3chr11:44595168-44595179CCACACCCTCT+6.02
KLF5MA0599.1chr11:44594574-44594584GGGGCGGGGC-6.02
Nr5a2MA0505.1chr11:44596590-44596605AAACTCAAGGTCAGA+6.07
RREB1MA0073.1chr11:44596112-44596132CCCCAAAAAACCCCCCAAAC+6.52
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_04077chr11:44598483-44599411Brain_Anterior_Caudate
SE_05079chr11:44598005-44603311Brain_Cingulate_Gyrus
SE_05928chr11:44597456-44603224Brain_Hippocampus_Middle
SE_08038chr11:44598482-44603027Brain_Inferior_Temporal_Lobe
SE_10955chr11:44585347-44606263CD20
SE_14978chr11:44594539-44596937CD4_Memory_Primary_7pool
SE_18030chr11:44593108-44597614CD4p_CD25-_CD45ROp_Memory
SE_18030chr11:44597648-44601032CD4p_CD25-_CD45ROp_Memory
SE_18725chr11:44593177-44599224CD4p_CD25-_Il17-_PMAstim_Th
SE_19325chr11:44586077-44599410CD4p_CD25-_Il17p_PMAstim_Th17
SE_25709chr11:44586950-44600967DND41
SE_27056chr11:44594021-44601651Esophagus
SE_32002chr11:44594861-44597255Gastric
SE_32002chr11:44597892-44600000Gastric
SE_39624chr11:44593301-44602114Jurkat
SE_42483chr11:44594870-44596126Lung
SE_42483chr11:44597733-44598845Lung
SE_52138chr11:44594818-44597200Skeletal_Muscle_Myoblast
SE_53218chr11:44594138-44596110Small_Intestine
SE_55965chr11:44594177-44599445u87
SE_62566chr11:44577989-44637584Tonsil
SE_63922chr11:44594804-44597961HSMM
SE_65536chr11:44594271-44595894Pancreatic_islets
SE_65536chr11:44596629-44602221Pancreatic_islets
SE_66474chr11:44593301-44602114Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 9             
ChromosomeStartEnd
chr114459439244595143
chr114459514744595263
chr114459561044595895
chr114459592444597228
chr114459623144596678
chr114459684844597017
chr114459819344598247
chr114459834144598455
chr114459835744598490
Number: 1             
IDChromosomeStartEnd
GH11I044572chr114459390744601798
Enhancer Sequence
TGGAAGCCGG TGGAAGAAGG TGGCTTTACA TCTGGGGTCC AGAGGGCTTG CTGACTGGCC 60
TGTCCTGGAC CTGGCAGAGT TACCCGTCCC GCCACAGGAC GTGCTGGACA GGAGGCAGCC 120
TCCTGCAGGA CCAGGTAGCA GGAGCAGAGA ACAGCCCAGA CAGAACTCTC CCTGCGGGCA 180
ATTTGGCTCT GCGAGGGGCG GGGCCCCACT GAGTCTGCCC TATGTGTCTC TAAGACGAAC 240
CAATCATAAG CCTCCCAGGG CGTGGCGTGA AGCGGGGATT TGGTAGGGGA GCGCAGAGCG 300
AGGCCTGAGG TGTTTCCCTG GCAGAGGTCC CTCCACTGGG AAACAAACGG AGAGGGGAGT 360
ATGTGTTCCC ACGTGTACAC ATAAACCGTT TTGAATGATA CCTGGTATGA CGTAAGCACT 420
CAATAAATGT TTGTTGTTGC TGATAATAAC AATTGGTAAA TTATACTAGT ACAGTTGGAA 480
AACCACCTCC CACTCACTGT CTTAAAAGGT GGAATATAAG AATGCTTTTG CAGTGGGACC 540
TATGAGACAT CATCGTATAT AGAGGAAATA GAAACTTGGC AGGGGAGGTT TGATTTATCT 600
GAGGTCATGG AGCAAGTGGG TGTCTAGGCC TTGAGTCACC TTTGGACATG TAGATAGCCC 660
ACCTCCCTGA CCCCTGGCCT TTCTGAACAC ACAGCAGTGG AGTAACTGAG GCAGGGAGGA 720
TGTGTCCTCT ACTCTGAACT AGTCACTTAT TTTCCATCCG AAAGCCCCTC TTATCTGCTT 780
TCTCTGCCCC ACACCCTCTC CTGGCATGGT TGAGCAAGTC TCCTTGTTTG CCAGGAGACG 840
GTATGGCATG GCACTGTGGT TCTCAAAATG TGTGCCTATC AGGAATCCCT AACCATCCCT 900
GCAAGTTGCA GTCAGGGAAA CACTGGGGCT GTGCCTACAG CTTGGGGTTC TAGCTTCTCA 960
GGCATTGATG TCAGCCAGGC CTAGCTATGG GCACAGTGTC TGTTCACCTC TGGGCAAGTT 1020
TCTTGGCCTC TCAGAGTCTT GGTTTTTATG AGGATTAAAT GAGATAATGC TGGTAAAATG 1080
CTTCGTGGCA GGCCCAGGGA AGAGTGCACC CTCAATGAAG CCAGAGGTTA AGGGTGGTGA 1140
TGATGAGCAA AGGCTGCTCC TGTCATTACT TCTGGGGAAA TGATAGGGAG TCTTCCTGTC 1200
CGAAGGCTGA GGTCCCTGAT CTGGAGTGAG GGAGCTTTCC GGGGTTGCTT GAAGCTCTGC 1260
TGGGGGGTCA GCAGAAGACT TAGATTCTCT GTAGTCTTGG TCCCCAGACT ATCTGAACCC 1320
AGCCTTGAGC TGGGTGCTCT TGGCATAGAG TTGAGGGCAA AGTTGAGGGC TTACGTCTAG 1380
AGTCACAGGA TCTTGGTGTT GTGAGAAGCT CTGTGGTCCA TCCAGTCAAC CTACCTGCCC 1440
AGTCTGATCC CATGGACCAC ATCCAGCCTT TGCTCGCACA CCTCAAGGCT TGGAAAGCTC 1500
ATGATTTTTT ATTTCTGGAA AGAACTGACT CTTAGAAAAT AGGGGATAGA ATCTGAGCAA 1560
ACCCACCCAC CCTTGGCTTC CCCATTTTGA TCCTGATCTT GCTTGTTGGA ATTACACACA 1620
ATGTGGAAAC ACCCTGGTGG GACCAAATCT TGTAGCAGAA GACCCCAGGC CAGCGATTCT 1680
GACATAGGAA GGAGATTTTT CTTTTAAAAA CTTTATCTAA ACCAAATGGC TACCCCAAAA 1740
AACCCCCCAA ACTTTCTGAT TATTGAAGAA AGAGGGTTTT TTTTGTGTGT GTGGAAAAAT 1800
TCAGGCGGTA AAGAACAGAC CTGCAGGAGG AAATAACTGC TCAGAGATAA CTGCCGTGAG 1860
CAGTTTGGTG TTTTGGCCTT AAAGACACAC ACATACAAGA TTGGGATTGT ACCACACAAA 1920
CCACTTCCTG CACTGCCACT TTTGACTGAG TGCTGTATAG GGAGGGTTTT CCCATGTGAT 1980
TGAGCATTCT TCTCCAGCAA GTTTCCCAGC TCTGTAGTAT TGCACCATAG GAATCTTCTG 2040
TGACCTGGTT AAGCATTCCC CAGCCATTGC ACATTTAGGC CCTTTGAATT TTTCATTAGT 2100
ATCCACATTG CTATAATGAT CGCCTTGTCC CTATGTATAT TTTGTACTCA ACTCTAATGA 2160
GCTCCATGGA ATGAATTTCT AGAAGTGGCT TTCCAGCTCA GATGGTTTTT AAACTCAAGG 2220
TCAGAGGACC AGAATCTCCC ACCATAACCA GTCTCCCAGT TTCGCTTCAG CCCTACTGGT 2280
GGGGGAGCGT TCTGTCTGTC CCTGGTGCTA GTTGGCCTAC CCACAGGAGG AGGAGGAGCA 2340
GGCTTTTAGG GTATGTGTAT CTGTGAAAGA GAAGGAGATG GAGAAAGGCA GATAGATATA 2400
GGGGAGTGTT TTCTCTTCAA TTACAGTCTG ATTTTGACCC TCTCCTCTCT GGGAGCCTGT 2460
GGTGTCATTA ACTAATCATG GGCTCTCTTT ACTATTTAAT GACCTCTCCC CACAGTGACT 2520
CCTTCCTCCC CAACAGTCTC CTGGAAAGGA GGAGGTGGGA AGATGAGTCA GTGGGGGAAA 2580
GTTTCTCCAG AGTAGGTGGT GGGTGTTGCA GTGGTTCTCA AACTCTGACA TGCATCAGTC 2640
CCTTGGATGG CTTATGAAAG CACAGATTGC TTGGCCCCAC CCCCAGGTTT CTGATTCTGT 2700
GGGTCTGGGG TACTGCCTGA GAATGTGCAT TGCTAACACG TTCCCAGGGG ACGCTGCATC 2760
TGCTGGCCCT GGACCACACT TTGGGTACCA GTAAAGTAGT GGGATGGGGC AGGGTGGGGT 2820
TCTGTGGTGA GTTTCAGCTC CTGGTGTTGC TGACAGTAGG AACCTTGTCC TGTTTAATAA 2880
AGGCTCATCT TGTGAGGCCT GAACTCACCT TCCCCTCCTA CCCCCACCTC ACCACCCCTT 2940
CTCCCATGTG TCCTTTGTAT ATATTGGGAA CTTTCTGTGC AGGAGGACAA GAGGATTATC 3000
AGCATCCCCG TTTTACGGAA AAGAAAATTG AGTCTCTGAC AAGTGACATG CTGTGTCTAA 3060
GGATGTTGAA AGTAGGAGGG CTAGTACTGG AACCCTGGCG CTGTCACGTT CCCCACCTTG 3120
ACTTCTCCAG TGCAGGTCTG GTGCGGAAGC AGAGATGCCT TCCCTGAACA CTGCACCGGC 3180
CCCAAGTGAG AGGCCTGGGG AGGCAGATTC CTCCACACCA TCTCTGCGCT AGGATCTTGC 3240
TCCACTTCTT ATCCCCTGAC TGACACTTCA GTAACGTGAT CTTCTTCCAA GGTCTAGTGT 3300
TCTCCAGCAG TTTATGTTCC CAGTTATTGT TCTGGGCAGG TTTTCTAGGA AGCCAGGAAC 3360
TTTCTCCTGT CAAGCCTGGG CTTCGTCTGG CAGGCACAAC AGAGGGAAAA GAGAAAAGCC 3420
TCAGTTGTTG AGCATCTAAT GTGTACCAGG CCCTGTCCTG GACACTTTGC AGCCATAATG 3480
TCAGGTCAGC CACCCCAGGT AGGGGTTAAC ATCAGGTCCC ATTGTACAGA TGAGGAAACT 3540
GAGGGTCCAG GAGGTAAAAC AACTTACCCA AGTTCACAGA ACTGAAAGGG GCAGAGCTGG 3600
GCTTTTGATT TCAAACTCAA GGCTGGGGTC TGGTCTGGGA TGGCAGCAGG TCCTGTTCTG 3660
GAGGGAGCCG GGATGTGGAG TAAGCAGCCT CTGCCCCACC CGCCATCCAC GCAGAGACGG 3720
TCAGCCCAAG GGTCAAAGCT CTCTTGGGAT TCAGGGTCTT GCAGTGGGAG GGCACTGGCT 3780
GGTCACCGGG AGACCCCTTT CAAATCCTGC TCTGCTGCTG CCTGGCTGTG TGGCCTGGGG 3840
GCAAGTCACT GCCCAGTTTG GGACATCTGA GTCCTCCTTT CTCATAATGA TCCCTTATGC 3900
TTTACAGCTC TTGGCAGTGG ACATTTTCTC ATGTACTTAT TCTCCGTCCC TCAAGCCTTC 3960
CAGCACCCTG TGAAATAGGG CGGGCATTAT TACTAAGCCC ATTTTCACAG AGGATGAGGA 4020
TGACAGGGCA GGGAGTTGCC CAGGATCCCG TGGGCAGTTG AGGGATGGTA CAAGAGCTAA 4080
GACTGGAACC TGGGTTGTCT TTGCTGCCCA TCTTGAGCCC AGCCCCTAAG ACGGGAGAAC 4140
TCTTTCTCTC TATTCTCAGC CTTAGGATGA AGGATCCCAG AGCTCTTAGC TGGGCTGGTG 4200
GGTCCTGGGT ACAAGGGGCC CAGGATCCCA GGAAGGGCTG GCCTGGGATC TTCGCTGTTG 4260
GCCAAGAACC CATGGGGAGG CAAGATAGGG TAGTCCAGGC TGTCTCTGTT TCTGACTCCT 4320
GCCCAGGCCT TGCACGTGAG GTCCTTGGTG CTGTGGGGAA GGAGGGGTTC AGCCCAGGTT 4380
TTCCTCCCAG CTCGGCTGCT TGCTTCTCCT GGGAACTGTG CTTGTCCTCT AAAATGTATC 4440
ATGCAGAATT TTCCAGACTC TCACACATGG GTGCCTGGGC CCTGCAGTTT CACCTGAATG 4500
CCATCACTTC CTCCTGTCTT CCTCATTCTT CTACACCTGG CTCCAGCCAC CTTCTTCCCT 4560
CAGGGAAGAC TTGCTCCTCT GGCCAAGCCG ACTCAACTCT CTCGGGTTCT GTGCAGTGGG 4620
TGAACTGGCT GACCGGGTTG GTTAACTCCC CAGTGAGGCA TGAGAGCAGG GCCTGTGGCT 4680
GGTGTGGGTC CAAGCCCCTG CAGGGTCTGG CAGGGCATGC AGCTGAGTCT ATGCATGCTA 4740
GGGAAAGGTT AGCCTCAGAC 4760