EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS101-00519 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr1:17894850-17897980 
Target genes
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
AGAGGAAACC AGGGATCGGA GCAGTGGATG GCATCTGTGT CACAGCTGGC CTCAGCTGGG 60
ATCGAGCACA GAGCTCAGTC TCCTAAAAAT CCCTACCCAG GGCATGATGG TGACATGGCA 120
AAAAGGGGAA CCTGGGGGGC ACACTGGCAG GACCAGAGAT TGCTTCAGAG CAGAAATGAC 180
CTGGAGTAGA GTGGTCCCAT TTTTCACTGG GCAAGCAGTG GTGTCTCTGC CTGCAGGATG 240
TCGGGGGGTG CTTGAAGCTC ATTACACCCA GTGTGGCTTC CATGCCAAGG CAGAAGGAAT 300
ACTAGGGGGA GTTTAGGACC AGGCTGTGGG CGGCATCCGC ATTGTCTGGT TCCTCGTAAG 360
TCGCACCACA GGGTTGGTCA GCAGCAGTTC AGCTCTTGTT AAAGCTGATA GGGAAAGAGG 420
ACGGGTGTTT GGGAACAGTT CTCTTGGGGG ATCCTGGTCC CGGATTTGAC TTCAACTCAG 480
GACAACAGGA CTCAGGGCAA ATCCTTTTAA TGATTGAAGC CATCCCTCCC TGCTCTCCCT 540
CCCCCAACAC CTCCAGCCCA GTCTTCCCTG TCCCCTTCCC ACAGCCCCAG TCCGCATCTT 600
CTCAGATTGT GAAGTTAATT GCAAGGGAGT GGGATGGACC CATTGGCCTG ATCCTGATGG 660
ATCTTTCCAG TCACAGCTGA AAGACCTTGG GTCTAATCAT GGATCCACCT TTGATCAGAT 720
TCTTGGCTTT GAACAAATCT CTCTCCCTCT CTGAGCCTCA GTTTCCTCCT CTGTAAAACA 780
GGGTCAGGTA CCTGCCATTC GTGGGTTGGC TCTGCCCCTG GAGGAACTGG TGGGAGGATT 840
AGGGGAGGCA CCAGGCATCC CCTGGCCTGG AGCAGTGCTC AGAGCCAACT CCCGCCAGAG 900
GTGCCCCAGA ACAGCTGGAA CTGCACTCAC ACCCTTATCT GGGGAGGACA GCACATCACT 960
GAGGGGTGTG GTTTGAATCA TAAGTGCTGG CTGCTCTGAA TTCAGCCAGA GCTATCCTGG 1020
GCTGTGTGGC TGAGGGCCCC CGGGGGTCCT GGGGCTCCAT GCTGGGCTTG CATTTCAGGA 1080
GACCTCAGAT GCTGCTGGCC TGCTTGCCCT GCCGTTGTTG GGTGGGTTGA GCTGTTTTTA 1140
GCTCTAAGCT TTGCAAAGGC TGTTTCTTTC CTGCCCAGAG CTCCCTCGTG GGACAGAGTG 1200
AACAGGCCCC TCCCTGCCAG ACAGAGATTG GGCCTGAAGA AAGAGCTTGG AGCCAGATGG 1260
GACCCTGTGG GCTTTGAAAG GGAGGCCTGG TTTGCTCTCT GTGGCCTGCC AACCTGGGAC 1320
ACCGGTGCCC AGCCTTGCTC CTTCCCTGGG AAACTGAATA GACGCCAGGG TCTCACACCT 1380
GCCCCGTGGG AAAGGCTGGG GTATGTGCCT GCCTGGTGAC GGTGGCAGCC GCGGAGGCTC 1440
GCGGATCCTG TCCCCTTTGC CGGCCACATG CTTCTGACTC ATCAGAGGAA GAATGTGGTC 1500
TTTTTGGGAG AGAGTTTTTA AAAATAGTCC AAGTCCTCCT CTGGCCCTGT CCCACTCCTC 1560
CCCTTCTGAC CATTTCCTGG CATCAGCCCC AGACCTCTTT CCACTCTGGT TTTGGGGAAC 1620
TGCCCCTTTG CAACTTGGCT GTGAATCTGT TTGTGAACCT TACTGGGGAG GAGCTGTCCT 1680
GGGTGCAGGC TGGTTTCAGA AGGGAGGGGC CCAGCTGTGG CCGCCTCCTC CCCAGGGGCC 1740
CGACTTGGGA CGAGGGATTT CTGCATTCCT TTGGCAACTG TGCCTTGGGT CGCCTGTGTG 1800
TCAGGCCTGT GCCATGGGTG CAGATAAGAG CGGTGAACAG TGGTCACAGT CCTGCCTTCA 1860
TGGAGTCCAC ATTCTCATAG GAGGAAACTG ATAAATAACT AAAATTTGTA GTTGCCAGAG 1920
GTGTTAAATC CTGTGAGGAT GGGGACACTG GGTCAGGGCA TGTGTGTGGG CTGTCAGGAG 1980
AAGGCCTCTG ATACAGCGAC CTTGGAGCAG AGCCCTGAAG GTGAGGGCAG CAGTGTGTGG 2040
GTATCTGGGG GAACAGCATT TCAGGCAGTG GGAACAGCAA GTGCAAAGGC CCTGAGGCAG 2100
AAACATGCTT GGGGCATTCA GGGAGCTGGA AGGTGGTGGT GACTAGAGTG AGCTGTGTGG 2160
AGAGAGGTAG GACATGAAGT CGGGGGGGTT GTGGGGGCTC TGACACGTGG GGCCTCAGAG 2220
ATCAAGATGA GGGCTTGGGT CTTCCTTAAA TGAGGTGAGA AAACATTCCA GGCTCTGAGC 2280
GGAGGATGAA CTTGGCCGCT GTGCTGAGAA CAACATGTCA GGGCAGGGGT AGAGGTGAGA 2340
GCAGAGGGAC TGGTCAGGAG GCGTTTTGAA TAGCCCAGGT GAGAGATGAT GGTGGTTTGG 2400
GCCATGGTGG TACTGTGGAG GGGGTGAGAT GCGCTCGGAT TCTGGGCGTA TGTTGAAGGT 2460
AGAGCCAGCA GGTTTGCTGA AGGGTGGGCC CTGGGTGTGA GACAGAGGTG TCAAGGATGA 2520
CTCCAAGGTT TTGGCCTTAG CAGCTGGTGG GATGGTGCTA GCAAGCGGGA TGGGAAGACT 2580
GGGAGGAGCA GGGTTCTTTG TTCTGGCAGC ATGGTGATCA GGAGGTGGGT ATGGGCACGT 2640
TAAGGCTGAG ATGCCCGATC AATCACTGAG TGAAGACACA GAGCAGGCAG AGGGGCAGAG 2700
CCTGGAGTTC AAGGGCAGGA CAGGCTGGAG GCATCACTAT GGCCATGGCT TAGGACCCAC 2760
GAAGTGAGCC AGGTGACCCA GGTGGCCCAG GGAGGAGCCG CGGTGTAGCC TGAACCTGGG 2820
AACTGCCAAC CTGGAGGGAG GAAGGAGGAG CGGAGGAAGG GGAGCTGGAG CGAGACGTGA 2880
AAGAAGGGAG CAGCTGGCAG GTCAGGCAGA ATGGGGACCG AGATGCTCCT CTCTCCCCAT 2940
CCTGGTCCAT CAGAACCGGT GTAGTGGAGG CCGCAGGTGA CCTCGTGAGC TGGCTGGCAA 3000
AGCGGTGGGC ACACACTTGG TTGGGAATAG GTAGCTCAGC ACAGAATAGG AGACAGGGAC 3060
AGGAGACGGA GCATGGGCAC TCCTCGGGGA AGTCTTGTAA AGGGGAGCAG AGAAATGGGG 3120
TAGTGGGTGG 3130