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

TagContent
EnhancerAtlas ID
HS003-12133 
Organism
Homo sapiens 
Tissue/cell
A549 
Coordinate
chr12:123377460-123380490 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TBX20MA0689.1chr12:123379326-123379337AAGGTGTGAAG+6.32
TBX21MA0690.1chr12:123379326-123379336AAGGTGTGAA+6.02
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_03969chr12:123378347-123382252Brain_Anterior_Caudate
SE_04866chr12:123378014-123381129Brain_Cingulate_Gyrus
SE_05835chr12:123378317-123382379Brain_Hippocampus_Middle
SE_06752chr12:123378416-123382121Brain_Hippocampus_Middle_150
SE_07820chr12:123377652-123382166Brain_Inferior_Temporal_Lobe
SE_11355chr12:123370263-123387549CD20
SE_12882chr12:123377890-123381272CD34_Primary_RO01480
SE_13364chr12:123377729-123381249CD34_Primary_RO01536
SE_14078chr12:123377748-123381115CD34_Primary_RO01549
SE_15159chr12:123377713-123382228CD4_Memory_Primary_7pool
SE_20678chr12:123378661-123382215CD56
SE_23035chr12:123378384-123382215CD8_primiary
SE_23125chr12:123375217-123381177Colon_Crypt_1
SE_23796chr12:123377783-123378365Colon_Crypt_2
SE_23796chr12:123378754-123381142Colon_Crypt_2
SE_25026chr12:123377453-123381217Colon_Crypt_3
SE_26757chr12:123374175-123382269Esophagus
SE_28186chr12:123375358-123381384Fetal_Intestine
SE_29262chr12:123375484-123381295Fetal_Intestine_Large
SE_30119chr12:123377830-123381482Fetal_Muscle
SE_31427chr12:123376086-123381520Gastric
SE_35883chr12:123370374-123381488HMEC
SE_37349chr12:123370777-123381030HSMMtube
SE_40937chr12:123377739-123381766Left_Ventricle
SE_42306chr12:123377588-123378498Lung
SE_42306chr12:123378563-123382126Lung
SE_43888chr12:123371004-123381065MM1S
SE_47190chr12:123370007-123381847Panc1
SE_47585chr12:123377775-123378356Pancreas
SE_47585chr12:123378815-123381113Pancreas
SE_50159chr12:123375223-123378525Sigmoid_Colon
SE_50159chr12:123378569-123382200Sigmoid_Colon
SE_52477chr12:123377643-123381671Small_Intestine
SE_53586chr12:123378659-123382219Spleen
SE_61538chr12:123340041-123395084Toledo
SE_62830chr12:123354785-123387061Tonsil
SE_64309chr12:123375007-123380904NHEK
SE_65302chr12:123377277-123381543Pancreatic_islets
SE_66800chr12:123378078-123380484Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12123379083123379880
Enhancer Sequence
AGCTGGGTGT GATGGCGCAC ACCTGTGAGC CCTGCTACGC AGGAGGCTAA GGCACGAGAA 60
TCACTTGAAC CCAGGAGGCA GAGGTTGCAG TGCGCTGAGA TTGTACTACT GCACTCCAGC 120
TGGGCAACAG AGCAAGATCC TTTCTCAAAA AAAAAAAAAA AGGAAAAGGT AAATGTTTTT 180
TAGGCTAATT GCAAATCATA ATTTACTCAA CATTCTTGAA ATGGGATCCT AGTAACTTTC 240
AGGATGATCT GGTATTAATG ATTGTCAGTC ATCTTTCAAA AAGAGAACTA TTAATATAAG 300
TGATTAATTA TTGCAATTAC TTTTTATTGA GCCCTACTGA TGGGCTGTGT TAAGTACTAA 360
TAGGCATCAT CTCACCTGAT CCTCACTCTA TGAAATAGGT ATTACTGTCA TATTATCCTT 420
TTCCAACAGA TACTCAGGCA GGTGAAGTGA CTTGCCTGCA ATCACACAGC TGGGAAGCGG 480
CCAAGTCCAG TCTGGAGTGT GTGATTCCAA AACCAGAATG TTCTTTAACA CGCCATCACA 540
AATGTTCCAT TTGGTCAACA GTTCATAAAA TATTTTCTTC TATTGTGTCT CACAATTACC 600
CCCAACATAA GCCAATGCAT AGCATTACCA GATGAGTGAA ACTACCATGA CCAAAAATTT 660
CGGTTCACAT TACACCCATT CCGAGAAAGG CACACCACAC ATGACCAGGA CGACAGGATT 720
GACAGTGATC CTCGCTAGGT GAGCTAAGGT ATTTTGGTTT TCAAGTTGTT TCCTTGTTTT 780
AAAAGCACTA CACCCAGAAA AGCAAACTAC TGCTGAGTAA TTTAATGTGA ACTATGCAGG 840
CTTATCAAGT GGAGTCGCTC AGGCCTCAAT ACTTCTCTTG GGTATTCAGG TATGAAGGTC 900
ACTTTTACTC AAAAAAAAAA AAAAAAAAAA AAAATCCTGC CAGATGAATT TACCTTTCTC 960
TTTAAAAAAT AATCTTCAGG TTCTGAGGTA GAGGAAACAG GTGAGGTTGT CCCTAACAGC 1020
CTCCAAGTGA ACAGAATGAA CTTGATTCTT TCCACAAGCT TCCCTCCACT AAAGGCAGTT 1080
TATTTCTATT AATGTTCCAC CAACAAAGCT ACAGTACTCA GTTCTTACTG CAACAGAATA 1140
GTCACATATA CCAAAATAAC TTGTAGGCAG TGTTACACAT TAGAAAAATA TACCTATCAT 1200
TTTATTATTA AACCAGAAAA ACCCTGCTGA CAATCAACAA AAGGTCTCCC AGCAACTGAA 1260
AAGCAGAGAA ACTAAGCAAA GATTTTTTCT TTGGAGACAT GAAACTCATT CAGCTAAGAA 1320
GGATGGATTT TATCACTTAT TATTCTCCAA AATGGAAGGT GCCACATGGA GACCATAAAC 1380
GGGGTACACT GCATCTTGGA GCAACGTTAT TATGTGTCAA GTTACAAAGC CCATGAATAC 1440
AAGGGGTGTA TTAATGGAAA GACTGATACC ATCTTACTAC AGTGGCCTCT CTGTAGCTCC 1500
GGACAATGAT CTGTTGAGGG TTTTCCAGGG ATTTTGAATG TGCAACCTCC ATACAAGCTC 1560
TCTTTTAAGG GGGCTGGCTT GGTGCTGAAC AATCCCTCTT CGGAAAGAAA GCCAAAAGCC 1620
CCCACACGGG CTCCTGGGTG AGAGGCTCAG CACTGTAGGC GTGGGAAGGC TCAGACTTCA 1680
GAGACATAAA GGAGTGGTAG GTGGGCCAGG AAGAGCTGGG ATTAGCCTGG GCCCACCTGC 1740
CTGGAGGAGA ACCAGACCCA AAAGATCAGA CTTTCCGAGA ATGAGTCCAA ATGGGTTGAG 1800
AGAAAGGGAG CACACACTGC AAATCTGCAA GGATGAAGTC AGTTACCCGA GAGCAAACCA 1860
CACCTCAAGG TGTGAAGGAA GATAACCAGA AACAGGAGCT GGCACATGCC TTCCAGGGGC 1920
TGGGCAAGGC TTGACTCTCA GAGGTGAGGG TTGGCAGCCA GCCCCAAACC CCCATTTTAA 1980
CTTCTTCCTG AAACTGCTCC AGGAACCTTC CTTAGTCCCA GACACGTGGG ACGCAGTGGT 2040
ACAAAGCCAG CCACACTAAA TTTCCCACCT TCCCTTCCTC GGTGGAGGGG GCAACCCTTA 2100
CAGAAAAACG TATCCTGTCG CCACCCTTAG GCCCATCCAC GAACTCCCGT AACTCTGCTG 2160
GGGCCACTTC AAAAGAAGTC AGACTCCAGG GGCATTATTG GGACCCCTTA GATACATGGA 2220
ACCTTCAAAC CTTACCCTGG CTATGGTATG ACCATGGACT CCTGCCTCCA AACCCTGGGC 2280
TGGGGACCCT CGCCCAACCC TTAAAGAGCC TCAGAACCAC CTCATAGACT CAGCTACAGA 2340
CCCTCAGCCT CCCGAACCCA TCTTGGAACC CTCAATCCTC TCCTAAGAGT CCTATTTGGA 2400
TAGTCCACTC AGTCCCCCAA AACCTACTCT GATCCCCTAT AGCTGCCTCA GTCCCCCTGG 2460
TTGTCCCCAA CCTTTCCTCT CAAAGGAAAC CCCCCAACCT CTACCAGATC TAGCTCTTGG 2520
TCCCCCTCAG TCACCCCTAA TCCTCGCCTC CGACTCAGCC CTTATTACTC TCCCCGCTCC 2580
TCCGACCAAA CCAATCTCAG ATCCCCCCAG TTCCGTCCTC TTCCGCCTAG ACCCAACGAT 2640
AGCACTCTAA TCCCCAAATT CCCATTCCAG GCTCCCTAAT CTCCACTTCA GACCCAGCCT 2700
TAAGTCTTCA GACCCAGCCT TAAGTCCTCA GCCCCACAAA ACCTTGTCTC AGGACCCCCA 2760
ATCGGCTCCC CAAGCCCCGT CTCAGGACCC TTTTTCCCGC CTCCGCCCTA GTCTCGGTCC 2820
CCTCAGTGCC TCAAACCCCC TCTCAGGCCC CCTATTCCTG CCTAAGCACC AGTCGCGGTT 2880
CCCTGGCTCC CGCACCCCGC CCCAAGCGCC CCCATTTCTA GCCCAGTCCC CTCAACACGA 2940
CCGGAGGCGC CGCGGTCGCC TCCGCCTCCG GCCACCGTTC GAGGAGCGAA CCCCGCTCGA 3000
GGCCTCACAG CCGCCGCCTT AAGCCCAGCT 3030