Tag | Content |
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EnhancerAtlas ID | HS085-00089 |
Organism | Homo sapiens |
Tissue/cell | Heart |
Coordinate | chr1:17895480-17897790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr1:17897554-17897569 | GAGTTCAAGGGCAGG | + | 6.1 | REST | MA0138.2 | chr1:17896519-17896540 | GGAGCTGTCCTGGGTGCAGGC | - | 7.07 | ZNF263 | MA0528.1 | chr1:17897690-17897711 | GAAGGAGGAGCGGAGGAAGGG | + | 7.14 | ZNF263 | MA0528.1 | chr1:17897693-17897714 | GGAGGAGCGGAGGAAGGGGAG | + | 7.15 | ZNF263 | MA0528.1 | chr1:17897686-17897707 | GGAGGAAGGAGGAGCGGAGGA | + | 7.28 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_00612 | chr1:17885040-17898127 | Adipose_Nuclei | SE_01537 | chr1:17887238-17903710 | Aorta | SE_03096 | chr1:17894836-17897293 | Bladder | SE_06186 | chr1:17884729-17903611 | Brain_Hippocampus_Middle | SE_23081 | chr1:17894994-17898004 | Colon_Crypt_1 | SE_23747 | chr1:17895586-17898000 | Colon_Crypt_2 | SE_24767 | chr1:17895440-17896896 | Colon_Crypt_3 | SE_24767 | chr1:17897349-17897980 | Colon_Crypt_3 | SE_26139 | chr1:17893912-17897509 | Duodenum_Smooth_Muscle | SE_26573 | chr1:17889896-17898099 | Esophagus | SE_28131 | chr1:17895406-17896604 | Fetal_Intestine | SE_29073 | chr1:17895366-17896616 | Fetal_Intestine_Large | SE_31687 | chr1:17894075-17897582 | Gastric | SE_34117 | chr1:17894944-17897531 | HCC1954 | SE_40808 | chr1:17894012-17898190 | Left_Ventricle | SE_43031 | chr1:17890076-17897872 | Lung | SE_46963 | chr1:17894194-17897822 | Ovary | SE_47562 | chr1:17895380-17897212 | Pancreas | SE_50079 | chr1:17894046-17898025 | Sigmoid_Colon | SE_52601 | chr1:17894207-17897494 | Small_Intestine | SE_54767 | chr1:17885171-17898261 | Stomach_Smooth_Muscle | SE_57000 | chr1:17894996-17897983 | VACO_400 | SE_57435 | chr1:17895275-17896682 | VACO_503 | SE_65277 | chr1:17894892-17897819 | Pancreatic_islets | SE_68684 | chr1:17894864-17898084 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I017567 | chr1 | 17893806 | 17897918 |
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Enhancer Sequence | GGGATGGACC CATTGGCCTG ATCCTGATGG ATCTTTCCAG TCACAGCTGA AAGACCTTGG 60 GTCTAATCAT GGATCCACCT TTGATCAGAT TCTTGGCTTT GAACAAATCT CTCTCCCTCT 120 CTGAGCCTCA GTTTCCTCCT CTGTAAAACA GGGTCAGGTA CCTGCCATTC GTGGGTTGGC 180 TCTGCCCCTG GAGGAACTGG TGGGAGGATT AGGGGAGGCA CCAGGCATCC CCTGGCCTGG 240 AGCAGTGCTC AGAGCCAACT CCCGCCAGAG GTGCCCCAGA ACAGCTGGAA CTGCACTCAC 300 ACCCTTATCT GGGGAGGACA GCACATCACT GAGGGGTGTG GTTTGAATCA TAAGTGCTGG 360 CTGCTCTGAA TTCAGCCAGA GCTATCCTGG GCTGTGTGGC TGAGGGCCCC CGGGGGTCCT 420 GGGGCTCCAT GCTGGGCTTG CATTTCAGGA GACCTCAGAT GCTGCTGGCC TGCTTGCCCT 480 GCCGTTGTTG GGTGGGTTGA GCTGTTTTTA GCTCTAAGCT TTGCAAAGGC TGTTTCTTTC 540 CTGCCCAGAG CTCCCTCGTG GGACAGAGTG AACAGGCCCC TCCCTGCCAG ACAGAGATTG 600 GGCCTGAAGA AAGAGCTTGG AGCCAGATGG GACCCTGTGG GCTTTGAAAG GGAGGCCTGG 660 TTTGCTCTCT GTGGCCTGCC AACCTGGGAC ACCGGTGCCC AGCCTTGCTC CTTCCCTGGG 720 AAACTGAATA GACGCCAGGG TCTCACACCT GCCCCGTGGG AAAGGCTGGG GTATGTGCCT 780 GCCTGGTGAC GGTGGCAGCC GCGGAGGCTC GCGGATCCTG TCCCCTTTGC CGGCCACATG 840 CTTCTGACTC ATCAGAGGAA GAATGTGGTC TTTTTGGGAG AGAGTTTTTA AAAATAGTCC 900 AAGTCCTCCT CTGGCCCTGT CCCACTCCTC CCCTTCTGAC CATTTCCTGG CATCAGCCCC 960 AGACCTCTTT CCACTCTGGT TTTGGGGAAC TGCCCCTTTG CAACTTGGCT GTGAATCTGT 1020 TTGTGAACCT TACTGGGGAG GAGCTGTCCT GGGTGCAGGC TGGTTTCAGA AGGGAGGGGC 1080 CCAGCTGTGG CCGCCTCCTC CCCAGGGGCC CGACTTGGGA CGAGGGATTT CTGCATTCCT 1140 TTGGCAACTG TGCCTTGGGT CGCCTGTGTG TCAGGCCTGT GCCATGGGTG CAGATAAGAG 1200 CGGTGAACAG TGGTCACAGT CCTGCCTTCA TGGAGTCCAC ATTCTCATAG GAGGAAACTG 1260 ATAAATAACT AAAATTTGTA GTTGCCAGAG GTGTTAAATC CTGTGAGGAT GGGGACACTG 1320 GGTCAGGGCA TGTGTGTGGG CTGTCAGGAG AAGGCCTCTG ATACAGCGAC CTTGGAGCAG 1380 AGCCCTGAAG GTGAGGGCAG CAGTGTGTGG GTATCTGGGG GAACAGCATT TCAGGCAGTG 1440 GGAACAGCAA GTGCAAAGGC CCTGAGGCAG AAACATGCTT GGGGCATTCA GGGAGCTGGA 1500 AGGTGGTGGT GACTAGAGTG AGCTGTGTGG AGAGAGGTAG GACATGAAGT CGGGGGGGTT 1560 GTGGGGGCTC TGACACGTGG GGCCTCAGAG ATCAAGATGA GGGCTTGGGT CTTCCTTAAA 1620 TGAGGTGAGA AAACATTCCA GGCTCTGAGC GGAGGATGAA CTTGGCCGCT GTGCTGAGAA 1680 CAACATGTCA GGGCAGGGGT AGAGGTGAGA GCAGAGGGAC TGGTCAGGAG GCGTTTTGAA 1740 TAGCCCAGGT GAGAGATGAT GGTGGTTTGG GCCATGGTGG TACTGTGGAG GGGGTGAGAT 1800 GCGCTCGGAT TCTGGGCGTA TGTTGAAGGT AGAGCCAGCA GGTTTGCTGA AGGGTGGGCC 1860 CTGGGTGTGA GACAGAGGTG TCAAGGATGA CTCCAAGGTT TTGGCCTTAG CAGCTGGTGG 1920 GATGGTGCTA GCAAGCGGGA TGGGAAGACT GGGAGGAGCA GGGTTCTTTG TTCTGGCAGC 1980 ATGGTGATCA GGAGGTGGGT ATGGGCACGT TAAGGCTGAG ATGCCCGATC AATCACTGAG 2040 TGAAGACACA GAGCAGGCAG AGGGGCAGAG CCTGGAGTTC AAGGGCAGGA CAGGCTGGAG 2100 GCATCACTAT GGCCATGGCT TAGGACCCAC GAAGTGAGCC AGGTGACCCA GGTGGCCCAG 2160 GGAGGAGCCG CGGTGTAGCC TGAACCTGGG AACTGCCAAC CTGGAGGGAG GAAGGAGGAG 2220 CGGAGGAAGG GGAGCTGGAG CGAGACGTGA AAGAAGGGAG CAGCTGGCAG GTCAGGCAGA 2280 ATGGGGACCG AGATGCTCCT CTCTCCCCAT 2310
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