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

TagContent
EnhancerAtlas ID
HS116-08306 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr12:52418970-52421640 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr12:52419607-52419626TTACCAGCAGAGGGCACCA+7.85
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_01015chr12:52418988-52420568Adrenal_Gland
SE_01838chr12:52418905-52419813Aorta
SE_03795chr12:52419121-52419814Brain_Angular_Gyrus
SE_04021chr12:52417333-52420328Brain_Anterior_Caudate
SE_05176chr12:52418685-52420454Brain_Cingulate_Gyrus
SE_05966chr12:52416302-52421515Brain_Hippocampus_Middle
SE_07218chr12:52418556-52420183Brain_Hippocampus_Middle_150
SE_07944chr12:52416412-52420722Brain_Inferior_Temporal_Lobe
SE_19846chr12:52416375-52420362CD4p_CD25-_Il17p_PMAstim_Th17
SE_23310chr12:52417342-52420086Colon_Crypt_1
SE_23835chr12:52419074-52420096Colon_Crypt_2
SE_24905chr12:52418355-52420465Colon_Crypt_3
SE_26342chr12:52418035-52421120Duodenum_Smooth_Muscle
SE_27026chr12:52418650-52420166Esophagus
SE_27026chr12:52420173-52421403Esophagus
SE_30252chr12:52418982-52421234Fetal_Muscle
SE_34732chr12:52418799-52421674HeLa
SE_38567chr12:52415886-52420142HUVEC
SE_40781chr12:52418902-52421724Left_Ventricle
SE_44280chr12:52419085-52420211NHDF-Ad
SE_45503chr12:52419049-52419922NHLF
SE_46044chr12:52418960-52419980Osteoblasts
SE_47765chr12:52419277-52419701Pancreas
SE_48081chr12:52418617-52421907Psoas_Muscle
SE_48629chr12:52418463-52421761Right_Atrium
SE_49724chr12:52419076-52420106Right_Ventricle
SE_49724chr12:52420180-52421509Right_Ventricle
SE_50349chr12:52416625-52420920Sigmoid_Colon
SE_51135chr12:52418530-52421933Skeletal_Muscle
SE_52700chr12:52416626-52420911Small_Intestine
SE_53734chr12:52418788-52420608Spleen
SE_54908chr12:52418581-52420576Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr125241904352419671
chr125241910152420892
chr125241930152419935
Enhancer Sequence
GTAGCTGGGA TTCCAGGCGG CCGCCACCAC GCCCGGCTAA TTTGTCATAT TTTTAGTAGA 60
GATGGGGTTT CGCCATGTTG GCCAGGCTGG TCTCGAACTC CTGACCTCAG GTGATCCACC 120
TGCCTCGGCC TCCCAAACTG CTGGGATTAC AGGGGTGAGC CACCGCCCCA GGCCTCTTTC 180
GGCACTGCCC TCAACCACAT GGGCCTCACT GTTCTTCCGG CGTACCCAGA CTTTCCCCAT 240
CTCAGCGCCT TCCCACCGGT CCTGTGTTTC CATGGCCTTT CCCCGGGTAG GGGCCTTTCT 300
TTTCCTAGCT TCGCTCAGTT CCCTGCTACA TTGTCGCCTC CTCGCAGAAG CCGTCTCTGG 360
CCGTTCCGTA TCGCTAGCGC CCTCTATCAT TCGCTAGCAG CTCACCCGGC TCTGTTTTTC 420
TTCATTGCAC TTCTCGTTAT GTGCCGTTCT CTTATAAATG TTTTTGTCTT TATCCCTCCC 480
ATAGAAGACA CCTCCATGAA AGGCCAGGGC TTTCCGAGGT TCTTTTCCTC TGTGGTTCCT 540
AGAAGAGGGC CTGGCACATA GCCGGCCTTG GCTAGCTTTT TGCGTAAATG TGAAGGGATC 600
CACCTTCCTC CCTTATAAGA GGTAGCAGTA CCTCCTGTTA CCAGCAGAGG GCACCACCGT 660
ACAGCACTTG GGGGCCGCAG GGGATCCTGC TGGGATGGGA GGTATTTAAA AAGCCCACAG 720
GCCTCTCCTC CCATAATGTG GGCGCTCCCA CAGCTGGGAC CGGAAGCAGG AGGGCCCCCT 780
GCGCTAATCT GCCCTGGCAG CAGCGAGCTG GCACGCCCTG GGTGCATCAT CCGGTGTGCT 840
CTGGTGCCCA AGGTCGGAAT ACCCTCACTG GTGGCTTGGA CACACCCCTG AGCAGCTGAT 900
GCTTCTGGAC AGATCACACC CTGTCCCGGG CTCTCAAAAT GAGGGCAATG ACATGAGCTG 960
CACTGCTCGC TCACGCGTTT GCTGTGAGGT TGGGACAGGA GTGCATGGGA AATGTTTTAT 1020
GAATGTAAAC ATGGGACAAA TATAATTTAT GCACGCCTTT ATTGGTAGTG CAGCAGATTG 1080
ACAACAAACG AGGGGAGAAG ATAAGGTATT TAAAGGAAAT TGCAAGGCTA AATGAAGGTG 1140
GGAATTAAGA CAGTGAAGGA GAACGAAGAA GTTAAAAATA ACAACTACCT TTCACCAAGA 1200
GCTTATTAGG AGCCAAGGCA GAGGAAAGTG ATCTCCAAAC ATTGTCTAAT TATAGCCAAC 1260
ACTTACATGG TGCTGACCTC ATGCCAGGAA CTCTTTAAGT GCTTTATGCA TAAAAACTCA 1320
CTGGATCCTC ACAACAACTC AGGGAGGTAG GTCATATCGC TGTCCCGTTC TACACAAGGA 1380
AACTGAGGCC CGGACAGCTT AAGTGACTGG CCCAAGGCCA CATAGATAGA CAGGGCTGGG 1440
CAATCTGCCT CCTGGAATGT GCTCTTAAAG CCCCACAGTC ACAGCCACAC CAAAAGGGAG 1500
ATATTGTTAT TATCATTCCA TTTCCCAAAC AAGCAACTGA GGCTTAGCAG ATGTACAAAG 1560
CCCGCCTAAA GCCACACTGG GAATATGTGT ATTTGAGCCC AGCTTAACCA CCCACCAAAC 1620
TAGGCCTGCA GGAGCTAGGA GGGGCTTCAG GAATGTGCAC AGGTTCTCTC GGAGGGCAGC 1680
AGCAGACATA CCCACTCTTC CTCTGAGCGG GGAGGGGAAG GTGAGAGCAC AGAGGCTGGG 1740
CAGGGCTGAT GGGGTTGAGG AAGAGGCTGC TTGGTGGCCT CAACTCCATG GACCGCAGAT 1800
GGCCAGGCAT CTTCTGGCCA GGAAGTGAGA GGTGTGTTGA TAGGCACAGT GGCTGTCCAC 1860
AGGGATTCCA GCCAGAGCTG TGGGCCCCCC ACAAATCTCC ATAGGGAGAC TAGGGACTGA 1920
GGGGTGGGCC TTACAGTGGG AGGTGGGAGC AGCCCCATCC CTACCACAAG TGCCCCTTAG 1980
CCCAGCCCTG ACTTCCAGCC CGTTACATAA GCTGCTGCAT ACCCAGGCCT GGAAATAGCT 2040
GAGGCTGTAC CGGCTGGGCT GGGAGACGTG ATGAATGGTC CCCAGGAGCA TCAGCTGACC 2100
GCCCTGTGCT CCTGAAGTGA CCTGAGGGCC TGCCAGCAGC TCGGGTTACC CAGCTCTCCC 2160
TGGGAGGCAG CCCTGCCTGG TCTGCTGAGG ATGGCTCTGA TGTGATTCTG TGTCTGGACA 2220
TTTATGGTTC GAGTGCCCGC AGGATGGTCC CTCTCCCAAG CCTGAGCAGC TAAGGCAGCT 2280
CCCAGCCACG CTGTGCCCAC TGGCAGCCTC TGGATGCTGG GAGCCAGGGC CTTGCCCAGA 2340
GCAAGCACTT GGATCTCTGC AGACAGTCAG CACTGGGAGG GCTGAGAGCT CTGCTGCTCT 2400
GAGTCCTGTG CTAAGGGCCC GCAAGGAAAG AGGAAGAGGA GCCTGAGAAA CTCGGGGTGC 2460
ACGTGGGGGC TGCAGGTGTC ATTCCAGGGC TGCACTCCAC CCACATCCCC ATGCCTCCTG 2520
TTTCACGGCC CACTCTGTTA CTGAACTGGT GGCCCTGGGC ACAGGGGGGC ACCCACACAC 2580
TCTGATGCCC ACTGCAGAGG GCAGAGCCAC ACACCCCTCC AGGGACTAGG CACATACACC 2640
CTTACTTCTG AGAGTAACGT GGCTAGGCTC 2670