Tag | Content |
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EnhancerAtlas ID | HS116-31409 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr7:47492080-47494810 |
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 | chr7:47493210-47493538 | 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 | chr7:47491914-47494736 | 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 | TGTTCAACTA TGAGAAACAA CAGACTAAGA TTGTATCTCT ATTTATTTGT AACGAAATAG 60 TCACAGGATC CTGCCTCCCT GGCCAGGAGC TCAGGCTGGT TTGGAACCAT ATGGAAGGAG 120 GCAGCTCAGG AAGACTGGCA GCAGGGAGAG GTAAGCAACA CTCAGGGAGG ACACAGAGAT 180 GTCAGCATTT CCAAAGAAGT CGGAAGCTCC CCTTTGCTCT TCTCACAAAT AAGTTTCCCA 240 AGAAGGGGCA GATGGGGCGG ATGGTTCTTA GGACACAAGG TCCCACCGAA CATCTGCAGC 300 ATTGAAGTGA AAGGGGAAAA ATGACTTGGA AATGCCCCTT CACTGCAAAG CAGCCAGTAC 360 CGGAGGCCAC AGAGGAGGGT GGCCAGGGAC AGACAAAGTG CCCAGTGCCA GCCCAGCCGA 420 GAGGCGGCAC GTGGGGAGTT GGGAACTTAC TGTGCTGGGC CTGGGCAGGG ACCACCGGCC 480 AGGGCTGCTT TTCCCTTCCA GAAACAGCTC CTCCTACGTT TCGCTCCTTC CCCTGCTTTA 540 GTCAAGCACA CCCCTCTTCG TGTTAATGTC TCGGCAGCTC TGGGCATAAA GGAGGCAGCT 600 GGAATAGCCC ACCAGGTGGG AGAGCCTGGT GAGTGTGGGA GTCCCCAGAA CCACAGCCAG 660 GAGCAGCTGG CAGGTGTGCC CGGCCCCACG GTGAGCACGC AGGCATGGAG CTCACAGGAC 720 AATGTCCGCC CGGGGCTGAG GGCCAGCCTG CCGAGGGCCA GCCTGCCAAG GGCCTGAGGG 780 ACAGGAACAA GAACAGCGCT CTCCGGGAGA GCCTTCTGAC CAGGAAGCTG AGTGGCTGTG 840 CCTTCCTGGG GACTAGCCAC TAGGGAGAAC CGCCTCTCAA AAGTTCCCCC AGGAAAAACA 900 AAACCTACTT CGAGCTGCTG GGAGGGCAGG TTACTCACCT CTGTATCCCA GGTAACAGAT 960 GCCTGATGCC CACTGGCCTT CCTCCCTCCC TCTTTCCTTC CTCTCCCCCA ACCCCATTCT 1020 CTCCTTTACC ACTTCCTTCC TTAGTTCATT TTTGCTCCAC TTCATTCCAA ATAGAATTTG 1080 AGATGACTCA TCGAATGAAT TCAACATAAC TAAATAAAAT TTTTAAAATA AAAACCAAAC 1140 CAATAAACAA GCACAAAAAC AGGGTTAAAG ACAAGAGTGG CCAGGCCAGA GAGAAGGAAA 1200 GGTATGCAGC GAAACCTCAG TTATGGGAAT GAGGCACCAG ACGGTTCTGA GTTACAAAAC 1260 GGGAGATGGA GGCCGGATAC ACGGCAGATC TTGGTGACAT AGAGTCCCGG ACCTGCCCGA 1320 GGCGGGTTTA TTTCCTCACT TAGCACTCAG AGCTAAGAGG AAGGGTGGCC AGCCCGGGCC 1380 ACATCGTGTC CTCAGCTGTT AGACTCACCC AGGCAGCTGT TTAAACTGAT CTCACTGATC 1440 TCATGACTAC ATGGTCAGTC ACGTCCCTTT AACTGACAGG GAGATTTGTG TGTGCTTTTT 1500 TGTAACATCT TACATGCACT TACATTCTTT TATTTTTATC ACTTATTTCA TAACGAAAAC 1560 ATTTCTTCAC ATAGAAAAGT GGACCAAGGG AGGGGAGGTG GGGAGGGCCT CATTGGGCCC 1620 CCAGCATAAC CCTATCAGTG GGCAGGGTGT TCTGGGGGCG CCCATTCCAC TGGAAACCAC 1680 GTGGTGTCTC CTTCCAGGCT GAACACAAAC AGGGGGCCCC AGTTTATAAC TAGCCAGGGG 1740 TGCACTGCTC AGACCAGGCT CAGCTCCACA AGGCAGCCTG CGCTTCCTGC CACCTGCCCA 1800 CCATTTGGCA GGGGCAGACA CAGCAGTGAC GGCAGGGGGT CAAAATAGGA CCACCTGTCC 1860 CTTTACTGGC CACAGTCATC AGACCCGGAG ACACTAAACA GGACTTTAAC TCCTCCGAGC 1920 ATTGGTTTCC ACCTCTGTGA AACTAGCTGA CAACACCACC AGCCTCCCAG GATCTCTGTG 1980 GGGACTAAGA AGATGCCTCA AGGCACCAAG CCCAAGCCAG CAGCACTCAT CATCAGCCCT 2040 GGGGGAGAGA GGAGGGTTGC ATGTGTTGTT TCCAGTCCAA CTCCCGCATT TTACAATGGA 2100 GGAAAGGCCA TGGGGAGGGG CTGCTCTGGG GGGGCAACAG CTGGGCAGGG TGTGGCACCC 2160 TGAGGACAGG CCAGTTTATT CCTTACTTCA TGGTGACAGA AAACAGGCCG AGCCCTAGAG 2220 AGCCAGCTCT CTCAAAGTAC CCCCAATGGG AGTGTCCTCA ACTGCAGGCA GCGGCCAGCC 2280 AGGCAGAGCC AGGCAGGGGG CTCCCATCCA TAGGCGAGCA AGTTAGCAAG GGCGGCCTGG 2340 GAGGGAAGTG CCTTCTCTAG AAGGTGACAA CATTGTTAAT GAGCCCGTGT TAATGTCAGT 2400 CATCTCCGGA GTCTGAAAGT GCCCTGCAGC AGGTGGGAGG GGTTATGTAT GCTGAGTCCA 2460 CTCTGGAGTA TGCCCTGCAG AGCTGCGTTC TGTCCTGTTA GATGTCCCAC CCAAACTCAC 2520 ACAGATCCCC CTGCAGAGAG CCTGGAAACC AGCCCCTCAG GGCACAGCAC AGGCATCCCA 2580 AGGACAGCCC CACCAAACCC CCAGCATACA GATACCTGGT CCTGTCCACA TGGGATGTCG 2640 GGGGTGCTGA CGGGGGCAAG ACCCACAGAT GCTGACCACC ATGGGCCACA GAGATAGGTC 2700 TCTGGCCCTG CAGCCAGCTG GTTCCATACA 2730
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