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

TagContent
EnhancerAtlas ID
HS105-21015 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr12:123378750-123380490 
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: 35             
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_23796chr12:123378754-123381142Colon_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_42306chr12:123378563-123382126Lung
SE_43888chr12:123371004-123381065MM1S
SE_47190chr12:123370007-123381847Panc1
SE_47585chr12:123378815-123381113Pancreas
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
TTGGAGACAT GAAACTCATT CAGCTAAGAA GGATGGATTT TATCACTTAT TATTCTCCAA 60
AATGGAAGGT GCCACATGGA GACCATAAAC GGGGTACACT GCATCTTGGA GCAACGTTAT 120
TATGTGTCAA GTTACAAAGC CCATGAATAC AAGGGGTGTA TTAATGGAAA GACTGATACC 180
ATCTTACTAC AGTGGCCTCT CTGTAGCTCC GGACAATGAT CTGTTGAGGG TTTTCCAGGG 240
ATTTTGAATG TGCAACCTCC ATACAAGCTC TCTTTTAAGG GGGCTGGCTT GGTGCTGAAC 300
AATCCCTCTT CGGAAAGAAA GCCAAAAGCC CCCACACGGG CTCCTGGGTG AGAGGCTCAG 360
CACTGTAGGC GTGGGAAGGC TCAGACTTCA GAGACATAAA GGAGTGGTAG GTGGGCCAGG 420
AAGAGCTGGG ATTAGCCTGG GCCCACCTGC CTGGAGGAGA ACCAGACCCA AAAGATCAGA 480
CTTTCCGAGA ATGAGTCCAA ATGGGTTGAG AGAAAGGGAG CACACACTGC AAATCTGCAA 540
GGATGAAGTC AGTTACCCGA GAGCAAACCA CACCTCAAGG TGTGAAGGAA GATAACCAGA 600
AACAGGAGCT GGCACATGCC TTCCAGGGGC TGGGCAAGGC TTGACTCTCA GAGGTGAGGG 660
TTGGCAGCCA GCCCCAAACC CCCATTTTAA CTTCTTCCTG AAACTGCTCC AGGAACCTTC 720
CTTAGTCCCA GACACGTGGG ACGCAGTGGT ACAAAGCCAG CCACACTAAA TTTCCCACCT 780
TCCCTTCCTC GGTGGAGGGG GCAACCCTTA CAGAAAAACG TATCCTGTCG CCACCCTTAG 840
GCCCATCCAC GAACTCCCGT AACTCTGCTG GGGCCACTTC AAAAGAAGTC AGACTCCAGG 900
GGCATTATTG GGACCCCTTA GATACATGGA ACCTTCAAAC CTTACCCTGG CTATGGTATG 960
ACCATGGACT CCTGCCTCCA AACCCTGGGC TGGGGACCCT CGCCCAACCC TTAAAGAGCC 1020
TCAGAACCAC CTCATAGACT CAGCTACAGA CCCTCAGCCT CCCGAACCCA TCTTGGAACC 1080
CTCAATCCTC TCCTAAGAGT CCTATTTGGA TAGTCCACTC AGTCCCCCAA AACCTACTCT 1140
GATCCCCTAT AGCTGCCTCA GTCCCCCTGG TTGTCCCCAA CCTTTCCTCT CAAAGGAAAC 1200
CCCCCAACCT CTACCAGATC TAGCTCTTGG TCCCCCTCAG TCACCCCTAA TCCTCGCCTC 1260
CGACTCAGCC CTTATTACTC TCCCCGCTCC TCCGACCAAA CCAATCTCAG ATCCCCCCAG 1320
TTCCGTCCTC TTCCGCCTAG ACCCAACGAT AGCACTCTAA TCCCCAAATT CCCATTCCAG 1380
GCTCCCTAAT CTCCACTTCA GACCCAGCCT TAAGTCTTCA GACCCAGCCT TAAGTCCTCA 1440
GCCCCACAAA ACCTTGTCTC AGGACCCCCA ATCGGCTCCC CAAGCCCCGT CTCAGGACCC 1500
TTTTTCCCGC CTCCGCCCTA GTCTCGGTCC CCTCAGTGCC TCAAACCCCC TCTCAGGCCC 1560
CCTATTCCTG CCTAAGCACC AGTCGCGGTT CCCTGGCTCC CGCACCCCGC CCCAAGCGCC 1620
CCCATTTCTA GCCCAGTCCC CTCAACACGA CCGGAGGCGC CGCGGTCGCC TCCGCCTCCG 1680
GCCACCGTTC GAGGAGCGAA CCCCGCTCGA GGCCTCACAG CCGCCGCCTT AAGCCCAGCT 1740