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

TagContent
EnhancerAtlas ID
HS155-00185 
Organism
Homo sapiens 
Tissue/cell
Ovary 
Coordinate
chr1:17894800-17897920 
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
CATTAGAACA GCCCTGTGCA TGGTGATTCT TATAGTTGTC ATTGTATGGA AGAGGAAACC 60
AGGGATCGGA GCAGTGGATG GCATCTGTGT CACAGCTGGC CTCAGCTGGG ATCGAGCACA 120
GAGCTCAGTC TCCTAAAAAT CCCTACCCAG GGCATGATGG TGACATGGCA AAAAGGGGAA 180
CCTGGGGGGC ACACTGGCAG GACCAGAGAT TGCTTCAGAG CAGAAATGAC CTGGAGTAGA 240
GTGGTCCCAT TTTTCACTGG GCAAGCAGTG GTGTCTCTGC CTGCAGGATG TCGGGGGGTG 300
CTTGAAGCTC ATTACACCCA GTGTGGCTTC CATGCCAAGG CAGAAGGAAT ACTAGGGGGA 360
GTTTAGGACC AGGCTGTGGG CGGCATCCGC ATTGTCTGGT TCCTCGTAAG TCGCACCACA 420
GGGTTGGTCA GCAGCAGTTC AGCTCTTGTT AAAGCTGATA GGGAAAGAGG ACGGGTGTTT 480
GGGAACAGTT CTCTTGGGGG ATCCTGGTCC CGGATTTGAC TTCAACTCAG GACAACAGGA 540
CTCAGGGCAA ATCCTTTTAA TGATTGAAGC CATCCCTCCC TGCTCTCCCT CCCCCAACAC 600
CTCCAGCCCA GTCTTCCCTG TCCCCTTCCC ACAGCCCCAG TCCGCATCTT CTCAGATTGT 660
GAAGTTAATT GCAAGGGAGT GGGATGGACC CATTGGCCTG ATCCTGATGG ATCTTTCCAG 720
TCACAGCTGA AAGACCTTGG GTCTAATCAT GGATCCACCT TTGATCAGAT TCTTGGCTTT 780
GAACAAATCT CTCTCCCTCT CTGAGCCTCA GTTTCCTCCT CTGTAAAACA GGGTCAGGTA 840
CCTGCCATTC GTGGGTTGGC TCTGCCCCTG GAGGAACTGG TGGGAGGATT AGGGGAGGCA 900
CCAGGCATCC CCTGGCCTGG AGCAGTGCTC AGAGCCAACT CCCGCCAGAG GTGCCCCAGA 960
ACAGCTGGAA CTGCACTCAC ACCCTTATCT GGGGAGGACA GCACATCACT GAGGGGTGTG 1020
GTTTGAATCA TAAGTGCTGG CTGCTCTGAA TTCAGCCAGA GCTATCCTGG GCTGTGTGGC 1080
TGAGGGCCCC CGGGGGTCCT GGGGCTCCAT GCTGGGCTTG CATTTCAGGA GACCTCAGAT 1140
GCTGCTGGCC TGCTTGCCCT GCCGTTGTTG GGTGGGTTGA GCTGTTTTTA GCTCTAAGCT 1200
TTGCAAAGGC TGTTTCTTTC CTGCCCAGAG CTCCCTCGTG GGACAGAGTG AACAGGCCCC 1260
TCCCTGCCAG ACAGAGATTG GGCCTGAAGA AAGAGCTTGG AGCCAGATGG GACCCTGTGG 1320
GCTTTGAAAG GGAGGCCTGG TTTGCTCTCT GTGGCCTGCC AACCTGGGAC ACCGGTGCCC 1380
AGCCTTGCTC CTTCCCTGGG AAACTGAATA GACGCCAGGG TCTCACACCT GCCCCGTGGG 1440
AAAGGCTGGG GTATGTGCCT GCCTGGTGAC GGTGGCAGCC GCGGAGGCTC GCGGATCCTG 1500
TCCCCTTTGC CGGCCACATG CTTCTGACTC ATCAGAGGAA GAATGTGGTC TTTTTGGGAG 1560
AGAGTTTTTA AAAATAGTCC AAGTCCTCCT CTGGCCCTGT CCCACTCCTC CCCTTCTGAC 1620
CATTTCCTGG CATCAGCCCC AGACCTCTTT CCACTCTGGT TTTGGGGAAC TGCCCCTTTG 1680
CAACTTGGCT GTGAATCTGT TTGTGAACCT TACTGGGGAG GAGCTGTCCT GGGTGCAGGC 1740
TGGTTTCAGA AGGGAGGGGC CCAGCTGTGG CCGCCTCCTC CCCAGGGGCC CGACTTGGGA 1800
CGAGGGATTT CTGCATTCCT TTGGCAACTG TGCCTTGGGT CGCCTGTGTG TCAGGCCTGT 1860
GCCATGGGTG CAGATAAGAG CGGTGAACAG TGGTCACAGT CCTGCCTTCA TGGAGTCCAC 1920
ATTCTCATAG GAGGAAACTG ATAAATAACT AAAATTTGTA GTTGCCAGAG GTGTTAAATC 1980
CTGTGAGGAT GGGGACACTG GGTCAGGGCA TGTGTGTGGG CTGTCAGGAG AAGGCCTCTG 2040
ATACAGCGAC CTTGGAGCAG AGCCCTGAAG GTGAGGGCAG CAGTGTGTGG GTATCTGGGG 2100
GAACAGCATT TCAGGCAGTG GGAACAGCAA GTGCAAAGGC CCTGAGGCAG AAACATGCTT 2160
GGGGCATTCA GGGAGCTGGA AGGTGGTGGT GACTAGAGTG AGCTGTGTGG AGAGAGGTAG 2220
GACATGAAGT CGGGGGGGTT GTGGGGGCTC TGACACGTGG GGCCTCAGAG ATCAAGATGA 2280
GGGCTTGGGT CTTCCTTAAA TGAGGTGAGA AAACATTCCA GGCTCTGAGC GGAGGATGAA 2340
CTTGGCCGCT GTGCTGAGAA CAACATGTCA GGGCAGGGGT AGAGGTGAGA GCAGAGGGAC 2400
TGGTCAGGAG GCGTTTTGAA TAGCCCAGGT GAGAGATGAT GGTGGTTTGG GCCATGGTGG 2460
TACTGTGGAG GGGGTGAGAT GCGCTCGGAT TCTGGGCGTA TGTTGAAGGT AGAGCCAGCA 2520
GGTTTGCTGA AGGGTGGGCC CTGGGTGTGA GACAGAGGTG TCAAGGATGA CTCCAAGGTT 2580
TTGGCCTTAG CAGCTGGTGG GATGGTGCTA GCAAGCGGGA TGGGAAGACT GGGAGGAGCA 2640
GGGTTCTTTG TTCTGGCAGC ATGGTGATCA GGAGGTGGGT ATGGGCACGT TAAGGCTGAG 2700
ATGCCCGATC AATCACTGAG TGAAGACACA GAGCAGGCAG AGGGGCAGAG CCTGGAGTTC 2760
AAGGGCAGGA CAGGCTGGAG GCATCACTAT GGCCATGGCT TAGGACCCAC GAAGTGAGCC 2820
AGGTGACCCA GGTGGCCCAG GGAGGAGCCG CGGTGTAGCC TGAACCTGGG AACTGCCAAC 2880
CTGGAGGGAG GAAGGAGGAG CGGAGGAAGG GGAGCTGGAG CGAGACGTGA AAGAAGGGAG 2940
CAGCTGGCAG GTCAGGCAGA ATGGGGACCG AGATGCTCCT CTCTCCCCAT CCTGGTCCAT 3000
CAGAACCGGT GTAGTGGAGG CCGCAGGTGA CCTCGTGAGC TGGCTGGCAA AGCGGTGGGC 3060
ACACACTTGG TTGGGAATAG GTAGCTCAGC ACAGAATAGG AGACAGGGAC AGGAGACGGA 3120