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

TagContent
EnhancerAtlas ID
HS098-14846 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr12:123377710-123380490 
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
GGTATTAATG ATTGTCAGTC ATCTTTCAAA AAGAGAACTA TTAATATAAG TGATTAATTA 60
TTGCAATTAC TTTTTATTGA GCCCTACTGA TGGGCTGTGT TAAGTACTAA TAGGCATCAT 120
CTCACCTGAT CCTCACTCTA TGAAATAGGT ATTACTGTCA TATTATCCTT TTCCAACAGA 180
TACTCAGGCA GGTGAAGTGA CTTGCCTGCA ATCACACAGC TGGGAAGCGG CCAAGTCCAG 240
TCTGGAGTGT GTGATTCCAA AACCAGAATG TTCTTTAACA CGCCATCACA AATGTTCCAT 300
TTGGTCAACA GTTCATAAAA TATTTTCTTC TATTGTGTCT CACAATTACC CCCAACATAA 360
GCCAATGCAT AGCATTACCA GATGAGTGAA ACTACCATGA CCAAAAATTT CGGTTCACAT 420
TACACCCATT CCGAGAAAGG CACACCACAC ATGACCAGGA CGACAGGATT GACAGTGATC 480
CTCGCTAGGT GAGCTAAGGT ATTTTGGTTT TCAAGTTGTT TCCTTGTTTT AAAAGCACTA 540
CACCCAGAAA AGCAAACTAC TGCTGAGTAA TTTAATGTGA ACTATGCAGG CTTATCAAGT 600
GGAGTCGCTC AGGCCTCAAT ACTTCTCTTG GGTATTCAGG TATGAAGGTC ACTTTTACTC 660
AAAAAAAAAA AAAAAAAAAA AAAATCCTGC CAGATGAATT TACCTTTCTC TTTAAAAAAT 720
AATCTTCAGG TTCTGAGGTA GAGGAAACAG GTGAGGTTGT CCCTAACAGC CTCCAAGTGA 780
ACAGAATGAA CTTGATTCTT TCCACAAGCT TCCCTCCACT AAAGGCAGTT TATTTCTATT 840
AATGTTCCAC CAACAAAGCT ACAGTACTCA GTTCTTACTG CAACAGAATA GTCACATATA 900
CCAAAATAAC TTGTAGGCAG TGTTACACAT TAGAAAAATA TACCTATCAT TTTATTATTA 960
AACCAGAAAA ACCCTGCTGA CAATCAACAA AAGGTCTCCC AGCAACTGAA AAGCAGAGAA 1020
ACTAAGCAAA GATTTTTTCT TTGGAGACAT GAAACTCATT CAGCTAAGAA GGATGGATTT 1080
TATCACTTAT TATTCTCCAA AATGGAAGGT GCCACATGGA GACCATAAAC GGGGTACACT 1140
GCATCTTGGA GCAACGTTAT TATGTGTCAA GTTACAAAGC CCATGAATAC AAGGGGTGTA 1200
TTAATGGAAA GACTGATACC ATCTTACTAC AGTGGCCTCT CTGTAGCTCC GGACAATGAT 1260
CTGTTGAGGG TTTTCCAGGG ATTTTGAATG TGCAACCTCC ATACAAGCTC TCTTTTAAGG 1320
GGGCTGGCTT GGTGCTGAAC AATCCCTCTT CGGAAAGAAA GCCAAAAGCC CCCACACGGG 1380
CTCCTGGGTG AGAGGCTCAG CACTGTAGGC GTGGGAAGGC TCAGACTTCA GAGACATAAA 1440
GGAGTGGTAG GTGGGCCAGG AAGAGCTGGG ATTAGCCTGG GCCCACCTGC CTGGAGGAGA 1500
ACCAGACCCA AAAGATCAGA CTTTCCGAGA ATGAGTCCAA ATGGGTTGAG AGAAAGGGAG 1560
CACACACTGC AAATCTGCAA GGATGAAGTC AGTTACCCGA GAGCAAACCA CACCTCAAGG 1620
TGTGAAGGAA GATAACCAGA AACAGGAGCT GGCACATGCC TTCCAGGGGC TGGGCAAGGC 1680
TTGACTCTCA GAGGTGAGGG TTGGCAGCCA GCCCCAAACC CCCATTTTAA CTTCTTCCTG 1740
AAACTGCTCC AGGAACCTTC CTTAGTCCCA GACACGTGGG ACGCAGTGGT ACAAAGCCAG 1800
CCACACTAAA TTTCCCACCT TCCCTTCCTC GGTGGAGGGG GCAACCCTTA CAGAAAAACG 1860
TATCCTGTCG CCACCCTTAG GCCCATCCAC GAACTCCCGT AACTCTGCTG GGGCCACTTC 1920
AAAAGAAGTC AGACTCCAGG GGCATTATTG GGACCCCTTA GATACATGGA ACCTTCAAAC 1980
CTTACCCTGG CTATGGTATG ACCATGGACT CCTGCCTCCA AACCCTGGGC TGGGGACCCT 2040
CGCCCAACCC TTAAAGAGCC TCAGAACCAC CTCATAGACT CAGCTACAGA CCCTCAGCCT 2100
CCCGAACCCA TCTTGGAACC CTCAATCCTC TCCTAAGAGT CCTATTTGGA TAGTCCACTC 2160
AGTCCCCCAA AACCTACTCT GATCCCCTAT AGCTGCCTCA GTCCCCCTGG TTGTCCCCAA 2220
CCTTTCCTCT CAAAGGAAAC CCCCCAACCT CTACCAGATC TAGCTCTTGG TCCCCCTCAG 2280
TCACCCCTAA TCCTCGCCTC CGACTCAGCC CTTATTACTC TCCCCGCTCC TCCGACCAAA 2340
CCAATCTCAG ATCCCCCCAG TTCCGTCCTC TTCCGCCTAG ACCCAACGAT AGCACTCTAA 2400
TCCCCAAATT CCCATTCCAG GCTCCCTAAT CTCCACTTCA GACCCAGCCT TAAGTCTTCA 2460
GACCCAGCCT TAAGTCCTCA GCCCCACAAA ACCTTGTCTC AGGACCCCCA ATCGGCTCCC 2520
CAAGCCCCGT CTCAGGACCC TTTTTCCCGC CTCCGCCCTA GTCTCGGTCC CCTCAGTGCC 2580
TCAAACCCCC TCTCAGGCCC CCTATTCCTG CCTAAGCACC AGTCGCGGTT CCCTGGCTCC 2640
CGCACCCCGC CCCAAGCGCC CCCATTTCTA GCCCAGTCCC CTCAACACGA CCGGAGGCGC 2700
CGCGGTCGCC TCCGCCTCCG GCCACCGTTC GAGGAGCGAA CCCCGCTCGA GGCCTCACAG 2760
CCGCCGCCTT AAGCCCAGCT 2780