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

TagContent
EnhancerAtlas ID
HS110-01062 
Organism
Homo sapiens 
Tissue/cell
KATO3 
Coordinate
chr12:123377860-123380490 
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: 40             
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_23796chr12:123378428-123378701Colon_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
ATTACTGTCA TATTATCCTT TTCCAACAGA TACTCAGGCA GGTGAAGTGA CTTGCCTGCA 60
ATCACACAGC TGGGAAGCGG CCAAGTCCAG TCTGGAGTGT GTGATTCCAA AACCAGAATG 120
TTCTTTAACA CGCCATCACA AATGTTCCAT TTGGTCAACA GTTCATAAAA TATTTTCTTC 180
TATTGTGTCT CACAATTACC CCCAACATAA GCCAATGCAT AGCATTACCA GATGAGTGAA 240
ACTACCATGA CCAAAAATTT CGGTTCACAT TACACCCATT CCGAGAAAGG CACACCACAC 300
ATGACCAGGA CGACAGGATT GACAGTGATC CTCGCTAGGT GAGCTAAGGT ATTTTGGTTT 360
TCAAGTTGTT TCCTTGTTTT AAAAGCACTA CACCCAGAAA AGCAAACTAC TGCTGAGTAA 420
TTTAATGTGA ACTATGCAGG CTTATCAAGT GGAGTCGCTC AGGCCTCAAT ACTTCTCTTG 480
GGTATTCAGG TATGAAGGTC ACTTTTACTC AAAAAAAAAA AAAAAAAAAA AAAATCCTGC 540
CAGATGAATT TACCTTTCTC TTTAAAAAAT AATCTTCAGG TTCTGAGGTA GAGGAAACAG 600
GTGAGGTTGT CCCTAACAGC CTCCAAGTGA ACAGAATGAA CTTGATTCTT TCCACAAGCT 660
TCCCTCCACT AAAGGCAGTT TATTTCTATT AATGTTCCAC CAACAAAGCT ACAGTACTCA 720
GTTCTTACTG CAACAGAATA GTCACATATA CCAAAATAAC TTGTAGGCAG TGTTACACAT 780
TAGAAAAATA TACCTATCAT TTTATTATTA AACCAGAAAA ACCCTGCTGA CAATCAACAA 840
AAGGTCTCCC AGCAACTGAA AAGCAGAGAA ACTAAGCAAA GATTTTTTCT TTGGAGACAT 900
GAAACTCATT CAGCTAAGAA GGATGGATTT TATCACTTAT TATTCTCCAA AATGGAAGGT 960
GCCACATGGA GACCATAAAC GGGGTACACT GCATCTTGGA GCAACGTTAT TATGTGTCAA 1020
GTTACAAAGC CCATGAATAC AAGGGGTGTA TTAATGGAAA GACTGATACC ATCTTACTAC 1080
AGTGGCCTCT CTGTAGCTCC GGACAATGAT CTGTTGAGGG TTTTCCAGGG ATTTTGAATG 1140
TGCAACCTCC ATACAAGCTC TCTTTTAAGG GGGCTGGCTT GGTGCTGAAC AATCCCTCTT 1200
CGGAAAGAAA GCCAAAAGCC CCCACACGGG CTCCTGGGTG AGAGGCTCAG CACTGTAGGC 1260
GTGGGAAGGC TCAGACTTCA GAGACATAAA GGAGTGGTAG GTGGGCCAGG AAGAGCTGGG 1320
ATTAGCCTGG GCCCACCTGC CTGGAGGAGA ACCAGACCCA AAAGATCAGA CTTTCCGAGA 1380
ATGAGTCCAA ATGGGTTGAG AGAAAGGGAG CACACACTGC AAATCTGCAA GGATGAAGTC 1440
AGTTACCCGA GAGCAAACCA CACCTCAAGG TGTGAAGGAA GATAACCAGA AACAGGAGCT 1500
GGCACATGCC TTCCAGGGGC TGGGCAAGGC TTGACTCTCA GAGGTGAGGG TTGGCAGCCA 1560
GCCCCAAACC CCCATTTTAA CTTCTTCCTG AAACTGCTCC AGGAACCTTC CTTAGTCCCA 1620
GACACGTGGG ACGCAGTGGT ACAAAGCCAG CCACACTAAA TTTCCCACCT TCCCTTCCTC 1680
GGTGGAGGGG GCAACCCTTA CAGAAAAACG TATCCTGTCG CCACCCTTAG GCCCATCCAC 1740
GAACTCCCGT AACTCTGCTG GGGCCACTTC AAAAGAAGTC AGACTCCAGG GGCATTATTG 1800
GGACCCCTTA GATACATGGA ACCTTCAAAC CTTACCCTGG CTATGGTATG ACCATGGACT 1860
CCTGCCTCCA AACCCTGGGC TGGGGACCCT CGCCCAACCC TTAAAGAGCC TCAGAACCAC 1920
CTCATAGACT CAGCTACAGA CCCTCAGCCT CCCGAACCCA TCTTGGAACC CTCAATCCTC 1980
TCCTAAGAGT CCTATTTGGA TAGTCCACTC AGTCCCCCAA AACCTACTCT GATCCCCTAT 2040
AGCTGCCTCA GTCCCCCTGG TTGTCCCCAA CCTTTCCTCT CAAAGGAAAC CCCCCAACCT 2100
CTACCAGATC TAGCTCTTGG TCCCCCTCAG TCACCCCTAA TCCTCGCCTC CGACTCAGCC 2160
CTTATTACTC TCCCCGCTCC TCCGACCAAA CCAATCTCAG ATCCCCCCAG TTCCGTCCTC 2220
TTCCGCCTAG ACCCAACGAT AGCACTCTAA TCCCCAAATT CCCATTCCAG GCTCCCTAAT 2280
CTCCACTTCA GACCCAGCCT TAAGTCTTCA GACCCAGCCT TAAGTCCTCA GCCCCACAAA 2340
ACCTTGTCTC AGGACCCCCA ATCGGCTCCC CAAGCCCCGT CTCAGGACCC TTTTTCCCGC 2400
CTCCGCCCTA GTCTCGGTCC CCTCAGTGCC TCAAACCCCC TCTCAGGCCC CCTATTCCTG 2460
CCTAAGCACC AGTCGCGGTT CCCTGGCTCC CGCACCCCGC CCCAAGCGCC CCCATTTCTA 2520
GCCCAGTCCC CTCAACACGA CCGGAGGCGC CGCGGTCGCC TCCGCCTCCG GCCACCGTTC 2580
GAGGAGCGAA CCCCGCTCGA GGCCTCACAG CCGCCGCCTT AAGCCCAGCT 2630