EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS092-09101 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr11:44594510-44599320 
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: 8             
ChromosomeStartEnd
chr114459514744595263
chr114459561044595895
chr114459592444597228
chr114459623144596678
chr114459684844597017
chr114459819344598247
chr114459834144598455
chr114459835744598490
Number: 1             
IDChromosomeStartEnd
GH11I044572chr114459390744601798
Enhancer Sequence
CCAGGTAGCA GGAGCAGAGA ACAGCCCAGA CAGAACTCTC CCTGCGGGCA ATTTGGCTCT 60
GCGAGGGGCG GGGCCCCACT GAGTCTGCCC TATGTGTCTC TAAGACGAAC CAATCATAAG 120
CCTCCCAGGG CGTGGCGTGA AGCGGGGATT TGGTAGGGGA GCGCAGAGCG AGGCCTGAGG 180
TGTTTCCCTG GCAGAGGTCC CTCCACTGGG AAACAAACGG AGAGGGGAGT ATGTGTTCCC 240
ACGTGTACAC ATAAACCGTT TTGAATGATA CCTGGTATGA CGTAAGCACT CAATAAATGT 300
TTGTTGTTGC TGATAATAAC AATTGGTAAA TTATACTAGT ACAGTTGGAA AACCACCTCC 360
CACTCACTGT CTTAAAAGGT GGAATATAAG AATGCTTTTG CAGTGGGACC TATGAGACAT 420
CATCGTATAT AGAGGAAATA GAAACTTGGC AGGGGAGGTT TGATTTATCT GAGGTCATGG 480
AGCAAGTGGG TGTCTAGGCC TTGAGTCACC TTTGGACATG TAGATAGCCC ACCTCCCTGA 540
CCCCTGGCCT TTCTGAACAC ACAGCAGTGG AGTAACTGAG GCAGGGAGGA TGTGTCCTCT 600
ACTCTGAACT AGTCACTTAT TTTCCATCCG AAAGCCCCTC TTATCTGCTT TCTCTGCCCC 660
ACACCCTCTC CTGGCATGGT TGAGCAAGTC TCCTTGTTTG CCAGGAGACG GTATGGCATG 720
GCACTGTGGT TCTCAAAATG TGTGCCTATC AGGAATCCCT AACCATCCCT GCAAGTTGCA 780
GTCAGGGAAA CACTGGGGCT GTGCCTACAG CTTGGGGTTC TAGCTTCTCA GGCATTGATG 840
TCAGCCAGGC CTAGCTATGG GCACAGTGTC TGTTCACCTC TGGGCAAGTT TCTTGGCCTC 900
TCAGAGTCTT GGTTTTTATG AGGATTAAAT GAGATAATGC TGGTAAAATG CTTCGTGGCA 960
GGCCCAGGGA AGAGTGCACC CTCAATGAAG CCAGAGGTTA AGGGTGGTGA TGATGAGCAA 1020
AGGCTGCTCC TGTCATTACT TCTGGGGAAA TGATAGGGAG TCTTCCTGTC CGAAGGCTGA 1080
GGTCCCTGAT CTGGAGTGAG GGAGCTTTCC GGGGTTGCTT GAAGCTCTGC TGGGGGGTCA 1140
GCAGAAGACT TAGATTCTCT GTAGTCTTGG TCCCCAGACT ATCTGAACCC AGCCTTGAGC 1200
TGGGTGCTCT TGGCATAGAG TTGAGGGCAA AGTTGAGGGC TTACGTCTAG AGTCACAGGA 1260
TCTTGGTGTT GTGAGAAGCT CTGTGGTCCA TCCAGTCAAC CTACCTGCCC AGTCTGATCC 1320
CATGGACCAC ATCCAGCCTT TGCTCGCACA CCTCAAGGCT TGGAAAGCTC ATGATTTTTT 1380
ATTTCTGGAA AGAACTGACT CTTAGAAAAT AGGGGATAGA ATCTGAGCAA ACCCACCCAC 1440
CCTTGGCTTC CCCATTTTGA TCCTGATCTT GCTTGTTGGA ATTACACACA ATGTGGAAAC 1500
ACCCTGGTGG GACCAAATCT TGTAGCAGAA GACCCCAGGC CAGCGATTCT GACATAGGAA 1560
GGAGATTTTT CTTTTAAAAA CTTTATCTAA ACCAAATGGC TACCCCAAAA AACCCCCCAA 1620
ACTTTCTGAT TATTGAAGAA AGAGGGTTTT TTTTGTGTGT GTGGAAAAAT TCAGGCGGTA 1680
AAGAACAGAC CTGCAGGAGG AAATAACTGC TCAGAGATAA CTGCCGTGAG CAGTTTGGTG 1740
TTTTGGCCTT AAAGACACAC ACATACAAGA TTGGGATTGT ACCACACAAA CCACTTCCTG 1800
CACTGCCACT TTTGACTGAG TGCTGTATAG GGAGGGTTTT CCCATGTGAT TGAGCATTCT 1860
TCTCCAGCAA GTTTCCCAGC TCTGTAGTAT TGCACCATAG GAATCTTCTG TGACCTGGTT 1920
AAGCATTCCC CAGCCATTGC ACATTTAGGC CCTTTGAATT TTTCATTAGT ATCCACATTG 1980
CTATAATGAT CGCCTTGTCC CTATGTATAT TTTGTACTCA ACTCTAATGA GCTCCATGGA 2040
ATGAATTTCT AGAAGTGGCT TTCCAGCTCA GATGGTTTTT AAACTCAAGG TCAGAGGACC 2100
AGAATCTCCC ACCATAACCA GTCTCCCAGT TTCGCTTCAG CCCTACTGGT GGGGGAGCGT 2160
TCTGTCTGTC CCTGGTGCTA GTTGGCCTAC CCACAGGAGG AGGAGGAGCA GGCTTTTAGG 2220
GTATGTGTAT CTGTGAAAGA GAAGGAGATG GAGAAAGGCA GATAGATATA GGGGAGTGTT 2280
TTCTCTTCAA TTACAGTCTG ATTTTGACCC TCTCCTCTCT GGGAGCCTGT GGTGTCATTA 2340
ACTAATCATG GGCTCTCTTT ACTATTTAAT GACCTCTCCC CACAGTGACT CCTTCCTCCC 2400
CAACAGTCTC CTGGAAAGGA GGAGGTGGGA AGATGAGTCA GTGGGGGAAA GTTTCTCCAG 2460
AGTAGGTGGT GGGTGTTGCA GTGGTTCTCA AACTCTGACA TGCATCAGTC CCTTGGATGG 2520
CTTATGAAAG CACAGATTGC TTGGCCCCAC CCCCAGGTTT CTGATTCTGT GGGTCTGGGG 2580
TACTGCCTGA GAATGTGCAT TGCTAACACG TTCCCAGGGG ACGCTGCATC TGCTGGCCCT 2640
GGACCACACT TTGGGTACCA GTAAAGTAGT GGGATGGGGC AGGGTGGGGT TCTGTGGTGA 2700
GTTTCAGCTC CTGGTGTTGC TGACAGTAGG AACCTTGTCC TGTTTAATAA AGGCTCATCT 2760
TGTGAGGCCT GAACTCACCT TCCCCTCCTA CCCCCACCTC ACCACCCCTT CTCCCATGTG 2820
TCCTTTGTAT ATATTGGGAA CTTTCTGTGC AGGAGGACAA GAGGATTATC AGCATCCCCG 2880
TTTTACGGAA AAGAAAATTG AGTCTCTGAC AAGTGACATG CTGTGTCTAA GGATGTTGAA 2940
AGTAGGAGGG CTAGTACTGG AACCCTGGCG CTGTCACGTT CCCCACCTTG ACTTCTCCAG 3000
TGCAGGTCTG GTGCGGAAGC AGAGATGCCT TCCCTGAACA CTGCACCGGC CCCAAGTGAG 3060
AGGCCTGGGG AGGCAGATTC CTCCACACCA TCTCTGCGCT AGGATCTTGC TCCACTTCTT 3120
ATCCCCTGAC TGACACTTCA GTAACGTGAT CTTCTTCCAA GGTCTAGTGT TCTCCAGCAG 3180
TTTATGTTCC CAGTTATTGT TCTGGGCAGG TTTTCTAGGA AGCCAGGAAC TTTCTCCTGT 3240
CAAGCCTGGG CTTCGTCTGG CAGGCACAAC AGAGGGAAAA GAGAAAAGCC TCAGTTGTTG 3300
AGCATCTAAT GTGTACCAGG CCCTGTCCTG GACACTTTGC AGCCATAATG TCAGGTCAGC 3360
CACCCCAGGT AGGGGTTAAC ATCAGGTCCC ATTGTACAGA TGAGGAAACT GAGGGTCCAG 3420
GAGGTAAAAC AACTTACCCA AGTTCACAGA ACTGAAAGGG GCAGAGCTGG GCTTTTGATT 3480
TCAAACTCAA GGCTGGGGTC TGGTCTGGGA TGGCAGCAGG TCCTGTTCTG GAGGGAGCCG 3540
GGATGTGGAG TAAGCAGCCT CTGCCCCACC CGCCATCCAC GCAGAGACGG TCAGCCCAAG 3600
GGTCAAAGCT CTCTTGGGAT TCAGGGTCTT GCAGTGGGAG GGCACTGGCT GGTCACCGGG 3660
AGACCCCTTT CAAATCCTGC TCTGCTGCTG CCTGGCTGTG TGGCCTGGGG GCAAGTCACT 3720
GCCCAGTTTG GGACATCTGA GTCCTCCTTT CTCATAATGA TCCCTTATGC TTTACAGCTC 3780
TTGGCAGTGG ACATTTTCTC ATGTACTTAT TCTCCGTCCC TCAAGCCTTC CAGCACCCTG 3840
TGAAATAGGG CGGGCATTAT TACTAAGCCC ATTTTCACAG AGGATGAGGA TGACAGGGCA 3900
GGGAGTTGCC CAGGATCCCG TGGGCAGTTG AGGGATGGTA CAAGAGCTAA GACTGGAACC 3960
TGGGTTGTCT TTGCTGCCCA TCTTGAGCCC AGCCCCTAAG ACGGGAGAAC TCTTTCTCTC 4020
TATTCTCAGC CTTAGGATGA AGGATCCCAG AGCTCTTAGC TGGGCTGGTG GGTCCTGGGT 4080
ACAAGGGGCC CAGGATCCCA GGAAGGGCTG GCCTGGGATC TTCGCTGTTG GCCAAGAACC 4140
CATGGGGAGG CAAGATAGGG TAGTCCAGGC TGTCTCTGTT TCTGACTCCT GCCCAGGCCT 4200
TGCACGTGAG GTCCTTGGTG CTGTGGGGAA GGAGGGGTTC AGCCCAGGTT TTCCTCCCAG 4260
CTCGGCTGCT TGCTTCTCCT GGGAACTGTG CTTGTCCTCT AAAATGTATC ATGCAGAATT 4320
TTCCAGACTC TCACACATGG GTGCCTGGGC CCTGCAGTTT CACCTGAATG CCATCACTTC 4380
CTCCTGTCTT CCTCATTCTT CTACACCTGG CTCCAGCCAC CTTCTTCCCT CAGGGAAGAC 4440
TTGCTCCTCT GGCCAAGCCG ACTCAACTCT CTCGGGTTCT GTGCAGTGGG TGAACTGGCT 4500
GACCGGGTTG GTTAACTCCC CAGTGAGGCA TGAGAGCAGG GCCTGTGGCT GGTGTGGGTC 4560
CAAGCCCCTG CAGGGTCTGG CAGGGCATGC AGCTGAGTCT ATGCATGCTA GGGAAAGGTT 4620
AGCCTCAGAC CTGTAACTCT CAGGCTTGTG ACTTTCAGCA AGTCACTTAT CTTCTCTGAA 4680
CCCTGGTTTC CTTCGTCGAA AAGTAAGGAA GCTACTTTCC TCGTTGATAG CTTCTGATAC 4740
TTTTAGGAGA TAAAGTGCAA AACATCTAGC ACTGGTGCCT GGGGGTTCAT GGTACTCAGG 4800
AAATGCCAGT 4810