EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS042-48868 
Organism
Homo sapiens 
Tissue/cell
Fetal_brain 
Coordinate
chr9:134531470-134533180 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESRRBMA0141.3chr9:134532487-134532498TCAAGGTCATT+6.32
EsrraMA0592.2chr9:134532486-134532497CTCAAGGTCAT+6.02
EsrrgMA0643.1chr9:134532487-134532497TCAAGGTCAT+6.02
SPI1MA0080.4chr9:134531976-134531990AACTTCCGCTTTCT-6.96
SPIBMA0081.2chr9:134531976-134531988AACTTCCGCTTT-6.22
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00600chr9:134529636-134532962Adipose_Nuclei
SE_00600chr9:134533009-134534664Adipose_Nuclei
SE_01504chr9:134531498-134534602Adrenal_Gland
SE_04540chr9:134530498-134532855Brain_Anterior_Caudate
SE_06320chr9:134530096-134534910Brain_Hippocampus_Middle
SE_09150chr9:134529296-134535237CD14
SE_10686chr9:134531167-134533203CD19_Primary
SE_10884chr9:134528077-134556344CD20
SE_12014chr9:134531280-134533216CD3
SE_14581chr9:134531143-134534806CD4_Memory_Primary_7pool
SE_15624chr9:134531417-134532953CD4_Memory_Primary_8pool
SE_16556chr9:134530983-134533667CD4_Naive_Primary_8pool
SE_17141chr9:134531244-134533028CD4p_CD225int_CD127p_Tmem
SE_17890chr9:134530053-134535085CD4p_CD25-_CD45ROp_Memory
SE_18432chr9:134530067-134535432CD4p_CD25-_Il17-_PMAstim_Th
SE_19146chr9:134530180-134535353CD4p_CD25-_Il17p_PMAstim_Th17
SE_20056chr9:134530416-134533758CD56
SE_21207chr9:134531102-134532913CD8_Memory_7pool
SE_22470chr9:134531101-134533555CD8_primiary
SE_23657chr9:134531582-134534613Colon_Crypt_1
SE_24289chr9:134531675-134532881Colon_Crypt_2
SE_24289chr9:134532889-134533311Colon_Crypt_2
SE_27117chr9:134531475-134532656Esophagus
SE_31710chr9:134531436-134534599Gastric
SE_36915chr9:134531091-134535736HSMMtube
SE_38112chr9:134529997-134535554HUVEC
SE_39729chr9:134531391-134534729Jurkat
SE_40722chr9:134531421-134535332Left_Ventricle
SE_42319chr9:134529786-134534755Lung
SE_50185chr9:134529549-134534764Sigmoid_Colon
SE_52495chr9:134529696-134534757Small_Intestine
SE_58352chr9:134520171-134620333Ly1
SE_58917chr9:134494900-134562990Ly3
SE_60991chr9:134494570-134620113HBL1
SE_62218chr9:134495530-134621458Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9134532379134532786
chr9134531700134532321
Number: 1             
IDChromosomeStartEnd
GH09I131653chr9134528775134535386
Enhancer Sequence
TGCCTGGCAC ACGGCACCCG CTCAACACAA GGAGCTTGGA TGCATAGCAA GGTCGATAGA 60
TACCGAATTC TTATTTCCCA GCTGCTTCCA GATCTTCATC CAGTTATTCT GCAACACTGA 120
ACATTTAACT CACTATTCTA AGTAAATGAG ACCTTATAAA TGCCCACTCT TCTCTTCCTT 180
TGGCACTGAA CCAGAAGTCT CAATCTGGCT TTTAGCCTAT TAGTCTATTT CCCTCTTTGG 240
TTTAACCTGC CTCCCTGCAT ACGGATCCTA TTGCTGTCCC TACTCCATGT CTTCTGATGG 300
CAGCCCCACA GTGTCCCTAA AAGACACAGC CTCTTCCCTC ACCAGGCAGG TTCCCAAGTC 360
AGATGGGCTG TCAGAGCAGT TTCCTAATCC ATGTGACTTG TATCCTGTTG AGTAGGACTG 420
AAGCAGGGAA AGCAGACACA AATGGGGAAG TCTGGGCAGG ATGCGTGGGT TCTCTGGTGC 480
TCAAAGATCT TCAGGCTGGG TGAGCCAACT TCCGCTTTCT CCACTGTCTA CTGCCCTGAG 540
TTGCTGTTCA GGCAGGCATG GGGCTGAGGA GCTGGCAAGA TTCACAACTG CGCCGTCATG 600
ACCACGGCGG AACTGGGGTA GACAAGTGAG GTGTAGAGGT CGATCACCAA AAAACCCTCT 660
CAGGTTCATG CAAGGGCAGG GACCAACTAA GGGCACTTCT GCCTATGAGC TGTTGATGGA 720
ACTCAAGAGG TTTATTATTG CACTCACAAT TCTTGTCTGC CTTGGGCAAG GCTGGGAAAA 780
CATGTCAGCA CCTAAAGACA GTGCAATGCC TACCAATAAA TCTCCCTCCT CAGGGTATCC 840
ACCTCAGCAC AGCCAGCTCT AGCACAAGAA GCCATAAATC AGGCAGAGAG AAGAGATTCT 900
TTCAAATGAC AACCAACCTT CTCAACGCTG GAAATCGAGG ACAGCACTAA CTAGGACAGT 960
ATGTTTGTCA CATCCTTCTT GAAACCTTGG GTTAGCAGCA CAGGCTTCAG GTGATTCTCA 1020
AGGTCATTCA CACTATGCCT TTGAGTGCTG AGGAGGTACT ATAATGCTTT GCGATAGCAG 1080
GGTGGGGAGG AAACGACAGG TGCCCTCACA TGAACACTGC TGTTAGGGCA ATCTCGCCAA 1140
CGGCTCCAGA CAGGCAGGCA GACAGACAGA CAGACAGACA GATGCACTCT CCCTGCCCCT 1200
TTCTCATGCA CGTCAATCAT CTGGGATGGA GGGCGACGTG AAGGGAGTGT TCCCACATGA 1260
CTGCTGCGTC GCAGGCAGTG CCACCAACTG CTCTCTTGCT ATTCCCCTGC TTTTCACACT 1320
TAGGAAGTTA CACTGTAGAA TTTGTATATG CGTCTCTTTA GTAATTTTCT AGAATTGAAG 1380
TTAAAACAAA AAATTTAAAG ATTTCATACA AATATATATA TGTACAAGTT ATAGAGAATG 1440
AATCAAATCC AGGCACCCAC CATCTGGCCT AGCAAACAGA ACCTTCTGCA GCGATGGAGG 1500
CGGCCGGTAC CTGAACTGTC TAACACGACA GGCACTAGTG GCTACTGAGG CCTGATTGTG 1560
GCTGCTGTGG CTGAGGCACT GAACTGTGAG TTAACTGTGT AAACAGCCCC TGGGGCTGGT 1620
GACTGGCACA CTGGATGGTG CAGCTCGAGA AGCGGATGGA TTCCACTGGT GCTGCCATGT 1680
GCTCCTCTAC AGCCACATCT CTTCCCTACA 1710