Tag | Content |
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EnhancerAtlas ID | HS161-13960 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr7:47491510-47494810 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr7:47493063-47493081 | CCCTCCCTCTTTCCTTCC | - | 6.63 | KLF4 | MA0039.3 | chr7:47494224-47494235 | GCAGGGTGTGG | - | 6.62 | Stat6 | MA0520.1 | chr7:47492265-47492280 | CATTTCCAAAGAAGT | + | 6.08 | ZNF263 | MA0528.1 | chr7:47493059-47493080 | TCCTCCCTCCCTCTTTCCTTC | - | 6.58 | ZNF263 | MA0528.1 | chr7:47493063-47493084 | CCCTCCCTCTTTCCTTCCTCT | - | 6.58 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_00125 | chr7:47491115-47495778 | Adipose_Nuclei | SE_00911 | chr7:47491995-47495703 | Adrenal_Gland | SE_01646 | chr7:47491862-47495094 | Aorta | SE_23406 | chr7:47492070-47494948 | Colon_Crypt_1 | SE_23979 | chr7:47492302-47493186 | Colon_Crypt_2 | SE_23979 | chr7:47493650-47494928 | Colon_Crypt_2 | SE_27919 | chr7:47492393-47494701 | Fetal_Intestine | SE_28808 | chr7:47492490-47494869 | Fetal_Intestine_Large | SE_31448 | chr7:47488264-47495617 | Gastric | SE_33716 | chr7:47490575-47494694 | H2171 | SE_36978 | chr7:47488216-47499271 | HSMMtube | SE_40936 | chr7:47491890-47494782 | Left_Ventricle | SE_42373 | chr7:47491874-47495601 | Lung | SE_46045 | chr7:47489368-47494878 | Osteoblasts | SE_46825 | chr7:47492386-47493105 | Ovary | SE_46825 | chr7:47493204-47494044 | Ovary | SE_47501 | chr7:47492117-47495034 | Pancreas | SE_48870 | chr7:47491970-47494936 | Right_Atrium | SE_50582 | chr7:47491938-47495031 | Sigmoid_Colon | SE_51778 | chr7:47488668-47495256 | Skeletal_Muscle_Myoblast | SE_52619 | chr7:47491084-47491913 | Small_Intestine | SE_52619 | chr7:47491914-47494736 | Small_Intestine | SE_53304 | chr7:47491863-47495190 | Spleen | SE_63537 | chr7:47488668-47495337 | HSMM | SE_65257 | chr7:47486917-47498821 | Pancreatic_islets |
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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 |
GH07I047449 | chr7 | 47488818 | 47495908 |
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Enhancer Sequence | AATACTAATG CCTGGGTAGG CAGCCAGCTC TACTGCTCGA GTAAGCCGTC TGATCTTGGG 60 AATTTACTTG CCCTCTGTGT GACTCAGTTT TCTCATCTGG AAAAGGGAGA CAGAAACAGC 120 ATTCTTGGAA GGATTAAATA AGGAAACATA AACATAGGGC TTAGAACAGT GCCTGGCCAG 180 TAATAAGTGC CAAAGAAATA TTAGCTACTT ATTCCATCAT CTTATTTCTG TGTCAGGCCT 240 CTGTGAGGCC CTGGAAATGC ACTTTATCCA CAAGTTATTA GGATCCCCCT TAGATCACAA 300 AACCAGCTGT GACCACAATG CCCATTTAAC AGTAGGAGAA ACAATGCTCA GAGAGGGTAA 360 GTGATTTTCC CAAAGCCACA CAGTTAATAA GACATTTTTT TCCCTTCCAG AACAAGAATA 420 CCAGGAACCA ATTAATTGTC AGGATTGCCC AACTTGATTT TCTGCTTAAT GCTTTTAAAC 480 ATAAGCAGCA ATCGTTAAGA ACTGCCAGAG AAAGTACACC CCATGGAGGG TGGGAAACTA 540 AAATAAAGTC ATCTTGTCAT TTTACCTTCA TGTTCAACTA TGAGAAACAA CAGACTAAGA 600 TTGTATCTCT ATTTATTTGT AACGAAATAG TCACAGGATC CTGCCTCCCT GGCCAGGAGC 660 TCAGGCTGGT TTGGAACCAT ATGGAAGGAG GCAGCTCAGG AAGACTGGCA GCAGGGAGAG 720 GTAAGCAACA CTCAGGGAGG ACACAGAGAT GTCAGCATTT CCAAAGAAGT CGGAAGCTCC 780 CCTTTGCTCT TCTCACAAAT AAGTTTCCCA AGAAGGGGCA GATGGGGCGG ATGGTTCTTA 840 GGACACAAGG TCCCACCGAA CATCTGCAGC ATTGAAGTGA AAGGGGAAAA ATGACTTGGA 900 AATGCCCCTT CACTGCAAAG CAGCCAGTAC CGGAGGCCAC AGAGGAGGGT GGCCAGGGAC 960 AGACAAAGTG CCCAGTGCCA GCCCAGCCGA GAGGCGGCAC GTGGGGAGTT GGGAACTTAC 1020 TGTGCTGGGC CTGGGCAGGG ACCACCGGCC AGGGCTGCTT TTCCCTTCCA GAAACAGCTC 1080 CTCCTACGTT TCGCTCCTTC CCCTGCTTTA GTCAAGCACA CCCCTCTTCG TGTTAATGTC 1140 TCGGCAGCTC TGGGCATAAA GGAGGCAGCT GGAATAGCCC ACCAGGTGGG AGAGCCTGGT 1200 GAGTGTGGGA GTCCCCAGAA CCACAGCCAG GAGCAGCTGG CAGGTGTGCC CGGCCCCACG 1260 GTGAGCACGC AGGCATGGAG CTCACAGGAC AATGTCCGCC CGGGGCTGAG GGCCAGCCTG 1320 CCGAGGGCCA GCCTGCCAAG GGCCTGAGGG ACAGGAACAA GAACAGCGCT CTCCGGGAGA 1380 GCCTTCTGAC CAGGAAGCTG AGTGGCTGTG CCTTCCTGGG GACTAGCCAC TAGGGAGAAC 1440 CGCCTCTCAA AAGTTCCCCC AGGAAAAACA AAACCTACTT CGAGCTGCTG GGAGGGCAGG 1500 TTACTCACCT CTGTATCCCA GGTAACAGAT GCCTGATGCC CACTGGCCTT CCTCCCTCCC 1560 TCTTTCCTTC CTCTCCCCCA ACCCCATTCT CTCCTTTACC ACTTCCTTCC TTAGTTCATT 1620 TTTGCTCCAC TTCATTCCAA ATAGAATTTG AGATGACTCA TCGAATGAAT TCAACATAAC 1680 TAAATAAAAT TTTTAAAATA AAAACCAAAC CAATAAACAA GCACAAAAAC AGGGTTAAAG 1740 ACAAGAGTGG CCAGGCCAGA GAGAAGGAAA GGTATGCAGC GAAACCTCAG TTATGGGAAT 1800 GAGGCACCAG ACGGTTCTGA GTTACAAAAC GGGAGATGGA GGCCGGATAC ACGGCAGATC 1860 TTGGTGACAT AGAGTCCCGG ACCTGCCCGA GGCGGGTTTA TTTCCTCACT TAGCACTCAG 1920 AGCTAAGAGG AAGGGTGGCC AGCCCGGGCC ACATCGTGTC CTCAGCTGTT AGACTCACCC 1980 AGGCAGCTGT TTAAACTGAT CTCACTGATC TCATGACTAC ATGGTCAGTC ACGTCCCTTT 2040 AACTGACAGG GAGATTTGTG TGTGCTTTTT TGTAACATCT TACATGCACT TACATTCTTT 2100 TATTTTTATC ACTTATTTCA TAACGAAAAC ATTTCTTCAC ATAGAAAAGT GGACCAAGGG 2160 AGGGGAGGTG GGGAGGGCCT CATTGGGCCC CCAGCATAAC CCTATCAGTG GGCAGGGTGT 2220 TCTGGGGGCG CCCATTCCAC TGGAAACCAC GTGGTGTCTC CTTCCAGGCT GAACACAAAC 2280 AGGGGGCCCC AGTTTATAAC TAGCCAGGGG TGCACTGCTC AGACCAGGCT CAGCTCCACA 2340 AGGCAGCCTG CGCTTCCTGC CACCTGCCCA CCATTTGGCA GGGGCAGACA CAGCAGTGAC 2400 GGCAGGGGGT CAAAATAGGA CCACCTGTCC CTTTACTGGC CACAGTCATC AGACCCGGAG 2460 ACACTAAACA GGACTTTAAC TCCTCCGAGC ATTGGTTTCC ACCTCTGTGA AACTAGCTGA 2520 CAACACCACC AGCCTCCCAG GATCTCTGTG GGGACTAAGA AGATGCCTCA AGGCACCAAG 2580 CCCAAGCCAG CAGCACTCAT CATCAGCCCT GGGGGAGAGA GGAGGGTTGC ATGTGTTGTT 2640 TCCAGTCCAA CTCCCGCATT TTACAATGGA GGAAAGGCCA TGGGGAGGGG CTGCTCTGGG 2700 GGGGCAACAG CTGGGCAGGG TGTGGCACCC TGAGGACAGG CCAGTTTATT CCTTACTTCA 2760 TGGTGACAGA AAACAGGCCG AGCCCTAGAG AGCCAGCTCT CTCAAAGTAC CCCCAATGGG 2820 AGTGTCCTCA ACTGCAGGCA GCGGCCAGCC AGGCAGAGCC AGGCAGGGGG CTCCCATCCA 2880 TAGGCGAGCA AGTTAGCAAG GGCGGCCTGG GAGGGAAGTG CCTTCTCTAG AAGGTGACAA 2940 CATTGTTAAT GAGCCCGTGT TAATGTCAGT CATCTCCGGA GTCTGAAAGT GCCCTGCAGC 3000 AGGTGGGAGG GGTTATGTAT GCTGAGTCCA CTCTGGAGTA TGCCCTGCAG AGCTGCGTTC 3060 TGTCCTGTTA GATGTCCCAC CCAAACTCAC ACAGATCCCC CTGCAGAGAG CCTGGAAACC 3120 AGCCCCTCAG GGCACAGCAC AGGCATCCCA AGGACAGCCC CACCAAACCC CCAGCATACA 3180 GATACCTGGT CCTGTCCACA TGGGATGTCG GGGGTGCTGA CGGGGGCAAG ACCCACAGAT 3240 GCTGACCACC ATGGGCCACA GAGATAGGTC TCTGGCCCTG CAGCCAGCTG GTTCCATACA 3300
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