EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS187-23640 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr8:28226720-28229640 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSMA0476.1chr8:28228855-28228866TCTGACTCATT+6.32
Foxd3MA0041.1chr8:28228702-28228714GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr8:28227572-28227584AAAAAAACATTC-6.52
NFAT5MA0606.1chr8:28227666-28227676ATTTTCCATT+6.02
NFATC1MA0624.1chr8:28227666-28227676ATTTTCCATT+6.02
NFATC3MA0625.1chr8:28227666-28227676ATTTTCCATT+6.02
Nr5a2MA0505.1chr8:28228314-28228329TAGTTCAAGGCCAGC+7.16
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00229chr8:28227525-28228529Adipose_Nuclei
SE_01444chr8:28226792-28227351Adrenal_Gland
SE_09976chr8:28227441-28229948CD14
SE_10881chr8:28219708-28248222CD20
SE_14002chr8:28226882-28229434CD34_Primary_RO01536
SE_17678chr8:28227433-28228879CD4p_CD25-_CD45RAp_Naive
SE_26645chr8:28226648-28227573Esophagus
SE_26645chr8:28227689-28229536Esophagus
SE_27701chr8:28220859-28228312Fetal_Intestine
SE_27701chr8:28228852-28234030Fetal_Intestine
SE_28577chr8:28220748-28235445Fetal_Intestine_Large
SE_31606chr8:28226832-28227525Gastric
SE_31606chr8:28228574-28229310Gastric
SE_36706chr8:28226411-28227963HMEC
SE_40988chr8:28226491-28227592Left_Ventricle
SE_42550chr8:28226724-28227568Lung
SE_42550chr8:28227670-28228551Lung
SE_47708chr8:28226906-28227577Pancreas
SE_48797chr8:28227685-28228525Right_Atrium
SE_52497chr8:28226685-28227591Small_Intestine
SE_53710chr8:28228490-28229198Spleen
SE_55734chr8:28226727-28228705u87
SE_58644chr8:28219872-28277477Ly1
SE_59813chr8:28219869-28277603Ly4
SE_61002chr8:28174118-28277761HBL1
SE_61739chr8:28219999-28279573Toledo
SE_62508chr8:28220381-28270893Tonsil
SE_65386chr8:28224811-28229860Pancreatic_islets
SE_67509chr8:28226727-28228705u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr82822674328227521
chr82822840028229533
Number: 1             
IDChromosomeStartEnd
GH08I028363chr82822052128234313
Enhancer Sequence
TTGAATGGAT CATCACATTC CCTGACAATG CCAAACAAAG GAGAATCACT CCTGAGGGTG 60
AAATGGTTAA AGGAGAAAAC TGGTTTGGAA CTCAAATGTC ACTTCAATGA ATGATCACAT 120
TATCTGACAA TGCCAAACCG ACAGGCAGGG GAGCCTGGCA GGAGGATGAG AGCTACCTGG 180
TGACTCACCT GGCTGGAATT AACATGTCAT AAAAAGGCAA CTGCCCTCTC CTTGCGGTGG 240
GTAATCAAGG CACCCATTTA GAGGCTTGCT GGTCAAAATG AACCAACTCC AGTGTTCCAT 300
GCTTGGAGCT CAACACTAAG TCAGACTGCT CTGGCCCTGG AGCCAAAGCC AGTGACCGAC 360
CCCTGCCCAT TACCCATGTG ACTAGGTGCC TGCCCCGCTC ACTTTCGGTA CCGGGTCTCT 420
TTCCTGCTCT GTTCCCCCAA GCCTGAATCT CAGCCTTGGG GCCCTGCCCT CAAGCCTCCC 480
CCAGGTGGGG CCTGGCCAGC CTCTGGGAGC TAATCCCGCC CACACGGGTG GGGGCAGACC 540
CACCTGGGGA GGGACTCACC GGAACCCCCG GGAAAGGGCC CCAGAGCAGA AAAAGCCCAG 600
CGTCTTTAAA CATATCAGCC CTGCTGCTAT GCAACATGTG GGTCCAGCTC TTGACCATGC 660
ACCAAACCAA ATATTAAGAA GCCTAAGAGT CAGACCCTGC CCTTAATGAA TTTGGGGCCT 720
AAATGAGCTA CCACCTGGTC CACACAGCCA GCACTTGTGT ATAAAAGCAC TTAATACGCT 780
CTGAAGCTAC ATTTATGTAC TGTGTTGTAT AATGAGATGA ATGAATGAAC ATTTGCATCT 840
CTCAGGAAAA TGAAAAAAAC ATTCAGCAAT CTGACACTGA AGCCTGATTT TTAAAAAGGG 900
GGTTTTTAGA ATGGAGCCCA TGAGTTAGAT GAATATCCAT GTGAACATTT TCCATTTTTG 960
ACATCAGTTA GATAAGTCAA AATAAAATAT GTTATGAATC TAAAAAAAAA AAATCCACTG 1020
AGTGACTGGA GGTTGAAGGA GACACAGGTT TCACCCCAAA AACAGAAAGT CAGCCTTAGT 1080
GACGAGAAGA CAGGCACCAT CGGGGAAGAT TTAAATACAT AGTGGAAAAT AAACGGAGTG 1140
GAGGAGGGGC TCGCCCAGGG CTCAAACCAC TAAGGAAGTG CCTTAAACGT ATTTTTCTCT 1200
GGAGGAAGCC ATTTAAGGAA TCTTTATGCC CCAATAACTG TGGGCATGAG AATGAGTTTC 1260
GAGACGAAAG AGAGATGGAG AAACAGGCTG AATGAGAGTT CACCCCAGTC CCAGCTTAGG 1320
ATGTTGGGGT GCCACTCTCT GAAGCTTTTC TTGAAATGGA TGGGGTGGCG GCATTAATCA 1380
GAAGCTGCTC ACTGGTGAGG ACGTTCTGAG CCCAAGTGAC AAAATAAATG TGCATCAATC 1440
GCAGACAGCA GCTGGCACAT ACTCTCCGAG TTTTCAGAGA AGGAAGGGAT AAAATCAGCA 1500
CCGGGTGCTG GTGAGTTCTG CCTGCCCCAG GAACACAACT GAGGGGGCTG ACACACACAC 1560
CCCCGCCACC TCAGGCCAGC AGGTAGACTG GACTTAGTTC AAGGCCAGCA GAAGAGGAGA 1620
ATCTTTTGAA GAAAAGGCAG TAGGATGTTC CCAAGAAATA AAATCACATC TAAGTGACAA 1680
GAGAATAACA GGAACCCTTA TATGTAATCC GTGGCCTTTC AAAGACTGAT GTGCATTCAG 1740
GAATGTTCTA ACAGCTATCA TTTATCAAAG ACTTAAGTGC CAGTCAACTT GCTGAGCATT 1800
TCGCAGACTG TGTCTCATTT AATCCCCCAC AAATAACCCA TGAGATTATA AATACCATCA 1860
TCATTCCCAT TTTACAGATG AGCAAACTGA ATCTCAGGGT GAGTAATTTT CCCAAGGCCA 1920
CGAAGCTAGA AAATGACAGA ACTCAGAATG TGAGCCCAAA TGTGTCTGAT TTCAAAAGCT 1980
ATGTTTGTTT GTTTTGAGAC AGGGTCTCCC TCTGCCACCC AGGCTGGAGT GCAGTCGCAC 2040
GATCACAGCT CACTGCGGCC TTGACCTCCC AGGTTCAAGC TATCCTGCCA CCTCAACCTC 2100
CCAAATAGCT GCGACTACAG GTGCGTGCCA CCACATCTGA CTCATTTTTG TATTTTTTGT 2160
AGAGACAGGA TTTCACCATG TTGCCAAGGC TTTTCTCGAA TTCCTGGGCT CAATCGATCC 2220
TCCTGCCTCG GCCTTCTAAA GTGCTAGGAT TACAGGTGTG AGCCACCAGA CCCAGACAAG 2280
CTATGCTCTT TCTACTATGT TGTACAGCCA GGAAATGTAT GCATCAAGTG ACAGACCAAA 2340
CTAGATGACC ACATAAGCTT CCTTGTTTTT AAAAACTTGA GTCACCAAGA GGCTAATGTG 2400
GTATTAGTGG TTGTGGCATG GAACGGGAAA TGTGCATTAT GACAGCAAAG AATCAAGCAT 2460
GGGATCCCCC AGGAGCAGGG CGACAATTCT TCTTATTTCA CCCTTTACAA ATATCCCAAA 2520
GAGAATGCAC AAACAGTCAG GGCTGCCTTA AGCTCAGACT TCCGGCTGGG CGCAGTGACT 2580
CACGCCTGTA ATCCCAGCAC TTTGGGAGGC CAAGGCAGGT GGATCACTTA AGGTGAGGAG 2640
TTCAAGACCA GCCTGACCAA CATAGCAAAA CCTCATCTCT ACTAAAAATA CAAAAGTTAC 2700
CTGGACATGA TGGTGGGCAC CTGCAATCCC AGCTACTGGG GAGGCTGAGG TATGAGAATT 2760
GCTTGTACCT AGGAGGTTGC AGTGAGTCAA AATCATGCCA CTGCACTCTA GCCTGGGTGA 2820
CAGAGTGAGA CCCTATCTCA AAAAAAAAAA TAGTTTTAAA AAAAAGCTCA AACTTCCCCA 2880
TTGTGACTTT GGCCAAATGA CCTCACCACT CTGTGCCTCA 2920