EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS043-00549 
Organism
Homo sapiens 
Tissue/cell
Fetal_heart 
Coordinate
chr1:17894810-17898060 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr5a2MA0505.1chr1:17897554-17897569GAGTTCAAGGGCAGG+6.1
RESTMA0138.2chr1:17896519-17896540GGAGCTGTCCTGGGTGCAGGC-7.07
ZNF263MA0528.1chr1:17897690-17897711GAAGGAGGAGCGGAGGAAGGG+7.14
ZNF263MA0528.1chr1:17897693-17897714GGAGGAGCGGAGGAAGGGGAG+7.15
ZNF263MA0528.1chr1:17897686-17897707GGAGGAAGGAGGAGCGGAGGA+7.28
ZNF263MA0528.1chr1:17895374-17895395CCTCCCTGCTCTCCCTCCCCC-7.68
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_00612chr1:17885040-17898127Adipose_Nuclei
SE_01537chr1:17887238-17903710Aorta
SE_03096chr1:17894836-17897293Bladder
SE_06186chr1:17884729-17903611Brain_Hippocampus_Middle
SE_23081chr1:17894994-17898004Colon_Crypt_1
SE_23747chr1:17895586-17898000Colon_Crypt_2
SE_24767chr1:17895440-17896896Colon_Crypt_3
SE_24767chr1:17897349-17897980Colon_Crypt_3
SE_26139chr1:17893912-17897509Duodenum_Smooth_Muscle
SE_26573chr1:17889896-17898099Esophagus
SE_28131chr1:17895406-17896604Fetal_Intestine
SE_29073chr1:17895366-17896616Fetal_Intestine_Large
SE_31687chr1:17894075-17897582Gastric
SE_34117chr1:17894944-17897531HCC1954
SE_40808chr1:17894012-17898190Left_Ventricle
SE_43031chr1:17890076-17897872Lung
SE_46963chr1:17894194-17897822Ovary
SE_47562chr1:17895380-17897212Pancreas
SE_50079chr1:17894046-17898025Sigmoid_Colon
SE_52601chr1:17894207-17897494Small_Intestine
SE_54767chr1:17885171-17898261Stomach_Smooth_Muscle
SE_57000chr1:17894996-17897983VACO_400
SE_57435chr1:17895275-17896682VACO_503
SE_65277chr1:17894892-17897819Pancreatic_islets
SE_68684chr1:17894864-17898084H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11789560017896843
Number: 1             
IDChromosomeStartEnd
GH01I017567chr11789380617897918
Enhancer Sequence
GCCCTGTGCA TGGTGATTCT TATAGTTGTC ATTGTATGGA AGAGGAAACC AGGGATCGGA 60
GCAGTGGATG GCATCTGTGT CACAGCTGGC CTCAGCTGGG ATCGAGCACA GAGCTCAGTC 120
TCCTAAAAAT CCCTACCCAG GGCATGATGG TGACATGGCA AAAAGGGGAA CCTGGGGGGC 180
ACACTGGCAG GACCAGAGAT TGCTTCAGAG CAGAAATGAC CTGGAGTAGA GTGGTCCCAT 240
TTTTCACTGG GCAAGCAGTG GTGTCTCTGC CTGCAGGATG TCGGGGGGTG CTTGAAGCTC 300
ATTACACCCA GTGTGGCTTC CATGCCAAGG CAGAAGGAAT ACTAGGGGGA GTTTAGGACC 360
AGGCTGTGGG CGGCATCCGC ATTGTCTGGT TCCTCGTAAG TCGCACCACA GGGTTGGTCA 420
GCAGCAGTTC AGCTCTTGTT AAAGCTGATA GGGAAAGAGG ACGGGTGTTT GGGAACAGTT 480
CTCTTGGGGG ATCCTGGTCC CGGATTTGAC TTCAACTCAG GACAACAGGA CTCAGGGCAA 540
ATCCTTTTAA TGATTGAAGC CATCCCTCCC TGCTCTCCCT CCCCCAACAC CTCCAGCCCA 600
GTCTTCCCTG TCCCCTTCCC ACAGCCCCAG TCCGCATCTT CTCAGATTGT GAAGTTAATT 660
GCAAGGGAGT GGGATGGACC CATTGGCCTG ATCCTGATGG ATCTTTCCAG TCACAGCTGA 720
AAGACCTTGG GTCTAATCAT GGATCCACCT TTGATCAGAT TCTTGGCTTT GAACAAATCT 780
CTCTCCCTCT CTGAGCCTCA GTTTCCTCCT CTGTAAAACA GGGTCAGGTA CCTGCCATTC 840
GTGGGTTGGC TCTGCCCCTG GAGGAACTGG TGGGAGGATT AGGGGAGGCA CCAGGCATCC 900
CCTGGCCTGG AGCAGTGCTC AGAGCCAACT CCCGCCAGAG GTGCCCCAGA ACAGCTGGAA 960
CTGCACTCAC ACCCTTATCT GGGGAGGACA GCACATCACT GAGGGGTGTG GTTTGAATCA 1020
TAAGTGCTGG CTGCTCTGAA TTCAGCCAGA GCTATCCTGG GCTGTGTGGC TGAGGGCCCC 1080
CGGGGGTCCT GGGGCTCCAT GCTGGGCTTG CATTTCAGGA GACCTCAGAT GCTGCTGGCC 1140
TGCTTGCCCT GCCGTTGTTG GGTGGGTTGA GCTGTTTTTA GCTCTAAGCT TTGCAAAGGC 1200
TGTTTCTTTC CTGCCCAGAG CTCCCTCGTG GGACAGAGTG AACAGGCCCC TCCCTGCCAG 1260
ACAGAGATTG GGCCTGAAGA AAGAGCTTGG AGCCAGATGG GACCCTGTGG GCTTTGAAAG 1320
GGAGGCCTGG TTTGCTCTCT GTGGCCTGCC AACCTGGGAC ACCGGTGCCC AGCCTTGCTC 1380
CTTCCCTGGG AAACTGAATA GACGCCAGGG TCTCACACCT GCCCCGTGGG AAAGGCTGGG 1440
GTATGTGCCT GCCTGGTGAC GGTGGCAGCC GCGGAGGCTC GCGGATCCTG TCCCCTTTGC 1500
CGGCCACATG CTTCTGACTC ATCAGAGGAA GAATGTGGTC TTTTTGGGAG AGAGTTTTTA 1560
AAAATAGTCC AAGTCCTCCT CTGGCCCTGT CCCACTCCTC CCCTTCTGAC CATTTCCTGG 1620
CATCAGCCCC AGACCTCTTT CCACTCTGGT TTTGGGGAAC TGCCCCTTTG CAACTTGGCT 1680
GTGAATCTGT TTGTGAACCT TACTGGGGAG GAGCTGTCCT GGGTGCAGGC TGGTTTCAGA 1740
AGGGAGGGGC CCAGCTGTGG CCGCCTCCTC CCCAGGGGCC CGACTTGGGA CGAGGGATTT 1800
CTGCATTCCT TTGGCAACTG TGCCTTGGGT CGCCTGTGTG TCAGGCCTGT GCCATGGGTG 1860
CAGATAAGAG CGGTGAACAG TGGTCACAGT CCTGCCTTCA TGGAGTCCAC ATTCTCATAG 1920
GAGGAAACTG ATAAATAACT AAAATTTGTA GTTGCCAGAG GTGTTAAATC CTGTGAGGAT 1980
GGGGACACTG GGTCAGGGCA TGTGTGTGGG CTGTCAGGAG AAGGCCTCTG ATACAGCGAC 2040
CTTGGAGCAG AGCCCTGAAG GTGAGGGCAG CAGTGTGTGG GTATCTGGGG GAACAGCATT 2100
TCAGGCAGTG GGAACAGCAA GTGCAAAGGC CCTGAGGCAG AAACATGCTT GGGGCATTCA 2160
GGGAGCTGGA AGGTGGTGGT GACTAGAGTG AGCTGTGTGG AGAGAGGTAG GACATGAAGT 2220
CGGGGGGGTT GTGGGGGCTC TGACACGTGG GGCCTCAGAG ATCAAGATGA GGGCTTGGGT 2280
CTTCCTTAAA TGAGGTGAGA AAACATTCCA GGCTCTGAGC GGAGGATGAA CTTGGCCGCT 2340
GTGCTGAGAA CAACATGTCA GGGCAGGGGT AGAGGTGAGA GCAGAGGGAC TGGTCAGGAG 2400
GCGTTTTGAA TAGCCCAGGT GAGAGATGAT GGTGGTTTGG GCCATGGTGG TACTGTGGAG 2460
GGGGTGAGAT GCGCTCGGAT TCTGGGCGTA TGTTGAAGGT AGAGCCAGCA GGTTTGCTGA 2520
AGGGTGGGCC CTGGGTGTGA GACAGAGGTG TCAAGGATGA CTCCAAGGTT TTGGCCTTAG 2580
CAGCTGGTGG GATGGTGCTA GCAAGCGGGA TGGGAAGACT GGGAGGAGCA GGGTTCTTTG 2640
TTCTGGCAGC ATGGTGATCA GGAGGTGGGT ATGGGCACGT TAAGGCTGAG ATGCCCGATC 2700
AATCACTGAG TGAAGACACA GAGCAGGCAG AGGGGCAGAG CCTGGAGTTC AAGGGCAGGA 2760
CAGGCTGGAG GCATCACTAT GGCCATGGCT TAGGACCCAC GAAGTGAGCC AGGTGACCCA 2820
GGTGGCCCAG GGAGGAGCCG CGGTGTAGCC TGAACCTGGG AACTGCCAAC CTGGAGGGAG 2880
GAAGGAGGAG CGGAGGAAGG GGAGCTGGAG CGAGACGTGA AAGAAGGGAG CAGCTGGCAG 2940
GTCAGGCAGA ATGGGGACCG AGATGCTCCT CTCTCCCCAT CCTGGTCCAT CAGAACCGGT 3000
GTAGTGGAGG CCGCAGGTGA CCTCGTGAGC TGGCTGGCAA AGCGGTGGGC ACACACTTGG 3060
TTGGGAATAG GTAGCTCAGC ACAGAATAGG AGACAGGGAC AGGAGACGGA GCATGGGCAC 3120
TCCTCGGGGA AGTCTTGTAA AGGGGAGCAG AGAAATGGGG TAGTGGGTGG AGAGGGTATG 3180
GGATCAGATG AGCAGTAATG CAGCGTATTT ATTCATTTAT TTATTATGAC TTTTTTGAGA 3240
TGGAGTCTTG 3250