Tag | Content |
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EnhancerAtlas ID | HS147-00585 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:17895410-17898250 |
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 | GTCTTCCCTG TCCCCTTCCC ACAGCCCCAG TCCGCATCTT CTCAGATTGT GAAGTTAATT 60 GCAAGGGAGT GGGATGGACC CATTGGCCTG ATCCTGATGG ATCTTTCCAG TCACAGCTGA 120 AAGACCTTGG GTCTAATCAT GGATCCACCT TTGATCAGAT TCTTGGCTTT GAACAAATCT 180 CTCTCCCTCT CTGAGCCTCA GTTTCCTCCT CTGTAAAACA GGGTCAGGTA CCTGCCATTC 240 GTGGGTTGGC TCTGCCCCTG GAGGAACTGG TGGGAGGATT AGGGGAGGCA CCAGGCATCC 300 CCTGGCCTGG AGCAGTGCTC AGAGCCAACT CCCGCCAGAG GTGCCCCAGA ACAGCTGGAA 360 CTGCACTCAC ACCCTTATCT GGGGAGGACA GCACATCACT GAGGGGTGTG GTTTGAATCA 420 TAAGTGCTGG CTGCTCTGAA TTCAGCCAGA GCTATCCTGG GCTGTGTGGC TGAGGGCCCC 480 CGGGGGTCCT GGGGCTCCAT GCTGGGCTTG CATTTCAGGA GACCTCAGAT GCTGCTGGCC 540 TGCTTGCCCT GCCGTTGTTG GGTGGGTTGA GCTGTTTTTA GCTCTAAGCT TTGCAAAGGC 600 TGTTTCTTTC CTGCCCAGAG CTCCCTCGTG GGACAGAGTG AACAGGCCCC TCCCTGCCAG 660 ACAGAGATTG GGCCTGAAGA AAGAGCTTGG AGCCAGATGG GACCCTGTGG GCTTTGAAAG 720 GGAGGCCTGG TTTGCTCTCT GTGGCCTGCC AACCTGGGAC ACCGGTGCCC AGCCTTGCTC 780 CTTCCCTGGG AAACTGAATA GACGCCAGGG TCTCACACCT GCCCCGTGGG AAAGGCTGGG 840 GTATGTGCCT GCCTGGTGAC GGTGGCAGCC GCGGAGGCTC GCGGATCCTG TCCCCTTTGC 900 CGGCCACATG CTTCTGACTC ATCAGAGGAA GAATGTGGTC TTTTTGGGAG AGAGTTTTTA 960 AAAATAGTCC AAGTCCTCCT CTGGCCCTGT CCCACTCCTC CCCTTCTGAC CATTTCCTGG 1020 CATCAGCCCC AGACCTCTTT CCACTCTGGT TTTGGGGAAC TGCCCCTTTG CAACTTGGCT 1080 GTGAATCTGT TTGTGAACCT TACTGGGGAG GAGCTGTCCT GGGTGCAGGC TGGTTTCAGA 1140 AGGGAGGGGC CCAGCTGTGG CCGCCTCCTC CCCAGGGGCC CGACTTGGGA CGAGGGATTT 1200 CTGCATTCCT TTGGCAACTG TGCCTTGGGT CGCCTGTGTG TCAGGCCTGT GCCATGGGTG 1260 CAGATAAGAG CGGTGAACAG TGGTCACAGT CCTGCCTTCA TGGAGTCCAC ATTCTCATAG 1320 GAGGAAACTG ATAAATAACT AAAATTTGTA GTTGCCAGAG GTGTTAAATC CTGTGAGGAT 1380 GGGGACACTG GGTCAGGGCA TGTGTGTGGG CTGTCAGGAG AAGGCCTCTG ATACAGCGAC 1440 CTTGGAGCAG AGCCCTGAAG GTGAGGGCAG CAGTGTGTGG GTATCTGGGG GAACAGCATT 1500 TCAGGCAGTG GGAACAGCAA GTGCAAAGGC CCTGAGGCAG AAACATGCTT GGGGCATTCA 1560 GGGAGCTGGA AGGTGGTGGT GACTAGAGTG AGCTGTGTGG AGAGAGGTAG GACATGAAGT 1620 CGGGGGGGTT GTGGGGGCTC TGACACGTGG GGCCTCAGAG ATCAAGATGA GGGCTTGGGT 1680 CTTCCTTAAA TGAGGTGAGA AAACATTCCA GGCTCTGAGC GGAGGATGAA CTTGGCCGCT 1740 GTGCTGAGAA CAACATGTCA GGGCAGGGGT AGAGGTGAGA GCAGAGGGAC TGGTCAGGAG 1800 GCGTTTTGAA TAGCCCAGGT GAGAGATGAT GGTGGTTTGG GCCATGGTGG TACTGTGGAG 1860 GGGGTGAGAT GCGCTCGGAT TCTGGGCGTA TGTTGAAGGT AGAGCCAGCA GGTTTGCTGA 1920 AGGGTGGGCC CTGGGTGTGA GACAGAGGTG TCAAGGATGA CTCCAAGGTT TTGGCCTTAG 1980 CAGCTGGTGG GATGGTGCTA GCAAGCGGGA TGGGAAGACT GGGAGGAGCA GGGTTCTTTG 2040 TTCTGGCAGC ATGGTGATCA GGAGGTGGGT ATGGGCACGT TAAGGCTGAG ATGCCCGATC 2100 AATCACTGAG TGAAGACACA GAGCAGGCAG AGGGGCAGAG CCTGGAGTTC AAGGGCAGGA 2160 CAGGCTGGAG GCATCACTAT GGCCATGGCT TAGGACCCAC GAAGTGAGCC AGGTGACCCA 2220 GGTGGCCCAG GGAGGAGCCG CGGTGTAGCC TGAACCTGGG AACTGCCAAC CTGGAGGGAG 2280 GAAGGAGGAG CGGAGGAAGG GGAGCTGGAG CGAGACGTGA AAGAAGGGAG CAGCTGGCAG 2340 GTCAGGCAGA ATGGGGACCG AGATGCTCCT CTCTCCCCAT CCTGGTCCAT CAGAACCGGT 2400 GTAGTGGAGG CCGCAGGTGA CCTCGTGAGC TGGCTGGCAA AGCGGTGGGC ACACACTTGG 2460 TTGGGAATAG GTAGCTCAGC ACAGAATAGG AGACAGGGAC AGGAGACGGA GCATGGGCAC 2520 TCCTCGGGGA AGTCTTGTAA AGGGGAGCAG AGAAATGGGG TAGTGGGTGG AGAGGGTATG 2580 GGATCAGATG AGCAGTAATG CAGCGTATTT ATTCATTTAT TTATTATGAC TTTTTTGAGA 2640 TGGAGTCTTG TTCTGTCACC CCAGCTGGAG TGCAGTAGTG CGATCTTGGC TCACTGCAAC 2700 CTCTGCCTCC TGGGTTCAAG TGATTCTCCT GCCTCAGCCT CCCGAGTAAC TGGGATTACA 2760 GGTGCCCGTC ACCACTCCCG GCTAATTTTT GTATTTTTAG TAGAGATAGG GTTTCACCAC 2820 CTTGACCAGG CTGGTCTTGG 2840
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