EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS094-43982 
Organism
Homo sapiens 
Tissue/cell
hMADS-3 
Coordinate
chr9:134532780-134534820 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxq1MA0040.1chr9:134533471-134533482AATAAACAATG-6.02
NKX2-3MA0672.1chr9:134534148-134534158TTCAAGTGGT-6.02
TCF7L2MA0523.1chr9:134534124-134534138AGACATCAAAGCCA+6.05
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00600chr9:134533009-134534664Adipose_Nuclei
SE_01504chr9:134531498-134534602Adrenal_Gland
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_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_22470chr9:134531101-134533555CD8_primiary
SE_23657chr9:134531582-134534613Colon_Crypt_1
SE_24289chr9:134532889-134533311Colon_Crypt_2
SE_24289chr9:134533407-134533811Colon_Crypt_2
SE_24289chr9:134534071-134534442Colon_Crypt_2
SE_27117chr9:134533321-134534611Esophagus
SE_29996chr9:134533624-134534596Fetal_Muscle
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_44268chr9:134533067-134534782NHDF-Ad
SE_50185chr9:134529549-134534764Sigmoid_Colon
SE_51828chr9:134533374-134534746Skeletal_Muscle_Myoblast
SE_52495chr9:134529696-134534757Small_Intestine
SE_58352chr9:134520171-134620333Ly1
SE_58917chr9:134494900-134562990Ly3
SE_60991chr9:134494570-134620113HBL1
SE_62218chr9:134495530-134621458Tonsil
SE_63616chr9:134533212-134534760HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9134534636134534723
Number: 1             
IDChromosomeStartEnd
GH09I131653chr9134528775134535386
Enhancer Sequence
TTTTCACACT TAGGAAGTTA CACTGTAGAA TTTGTATATG CGTCTCTTTA GTAATTTTCT 60
AGAATTGAAG TTAAAACAAA AAATTTAAAG ATTTCATACA AATATATATA TGTACAAGTT 120
ATAGAGAATG AATCAAATCC AGGCACCCAC CATCTGGCCT AGCAAACAGA ACCTTCTGCA 180
GCGATGGAGG CGGCCGGTAC CTGAACTGTC TAACACGACA GGCACTAGTG GCTACTGAGG 240
CCTGATTGTG GCTGCTGTGG CTGAGGCACT GAACTGTGAG TTAACTGTGT AAACAGCCCC 300
TGGGGCTGGT GACTGGCACA CTGGATGGTG CAGCTCGAGA AGCGGATGGA TTCCACTGGT 360
GCTGCCATGT GCTCCTCTAC AGCCACATCT CTTCCCTACA GGCAGCCCGA CTCTGACTTT 420
CAGACTTATC ATCCCTTACT TTTCAGGATA GTTTATATCG ACATATACAG TTTAACTTAT 480
AAGTTTGTGA ACGTTACCTA AGTGATGGCA TATTGTAAAG ATTCTCACGC TCTTGTTTTT 540
TACTCAATAG CAGGCCTGAC ACTCAGGCAT GCTGGGGTGT ATCAGTGATT TCGTTTTCAA 600
TGCTGAGAAA TTCCGTAGAT TCCATAATCC CAGCTTTATT TATCTGCTCT CCTGTCAGTG 660
GACACTGGGT CGCTTCCAGC ATTTTTGCTT TAATAAACAA TGCTGCTCAT ACATGTCTCC 720
TGGAACACAT GCCAACAGTC CTCTAAGAGC AGAACGGCTG GATTGTAGGG TATATGCCAC 780
ATTGATTCTT ACAGATATTG CAAAACAATT CTCCCAAGTG GCTATGCCAC TTTACAGTCC 840
CACTAGCAAG GTTGGGAGAG TCCTAGTTGC TCCATATTCC TCCCGGCACC TGGGGTTGCC 900
AGACATGCAA ACTTTCCCAC ATGGCCATGT CTAAGAAAGG ACACAAAAGT CCTCCTTCAC 960
CTGGAAATGC CATATGCTGG TGTATTTTAT TGTGATCTAT CTAATCTGTG AGAGCAACTT 1020
CAAGTTCACC TGAACTTGAG AACAGAAAGC CTCAGACTCT TGCTCCATGT TACATTTACC 1080
CCAAGGTCAG AGACTCCCAG TGACTAATCT GCTAGTCATT CCTTCCAGAG GAAGGGTGGC 1140
TTATATGAGC TTACAAACAA TTTCTGTATA AATTGACTGT GATGTTACCA ACAGCAGCCA 1200
CTTTCTTGGG CAACCATCGC AGGCTACAGA TCTGGCTGTC GGATGAATGT CCTTCTCTAC 1260
CGAGAGAGAA AGAGGATGGG CCGGAGGAGA GGATGTAGCC TGCTCACAGA ATCATGTCTC 1320
AACAGAAAAC CAAGCAGAGC AAAAAGACAT CAAAGCCAAC CCAATTTCTT CAAGTGGTCT 1380
GCCAGATGCC AATATTTCAT TCTTAAATTT TTAACTTGCC CCTCGGCCAG GCTTAACAAT 1440
GGTCTCTGCC TGTTGCTGAC AAATGTGGCT ATCAACTGGC CTTCTTTCTG TGTCATTTGT 1500
AGCAGCAGCT GGGTTCCCAA CTTAGCAGTG GTTTCTGTCT CAACTTAATC TCTCACCAGG 1560
GATGGTGGGG AGTCTCTAAA CATCAACCAC ACGGGATCAC AAAGTCAAGG GCAAGGTGGA 1620
CAACTTTGAG GCAGCCAATC TTGAGAAACG CTGTGGCTAA TTCCTCATTC CCTGTCTTCT 1680
ACTGGGCTCA GAAGTCGAGC ACTGGGAAGG ATTTAGAGAT CACTTACTTA ATAAACATTC 1740
CCCATTTTCC AAATGCATAA AAAGGACAAA TGGAGTGGAG GCGTGATTGA GGACATTAGG 1800
AAAAGCTTTT TTAAAGATGA GGATTTCCAA TTTTTTAAAA GTCTTTTCAC TTGTCTAGGA 1860
TTTTGTGGAC CGCAAGGTAA AGATGGAGAC AGAGGGCTAT GGGCACAGGA GGCAGCAGAG 1920
CTGAAGTCTG TGGCTTTTTT TTTAAATCTA TTTATTTATT TTATCTTGAG ACCAGGTTAC 1980
GAGACTGGCT AATTTTTGTA TTTTTGGTAG AGACAGGGTT TCGCCATGTT GCCTAGGTTG 2040