Tag | Content |
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EnhancerAtlas ID | HS155-12766 |
Organism | Homo sapiens |
Tissue/cell | Ovary |
Coordinate | chr7:47492120-47494590 |
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 | ATTTATTTGT AACGAAATAG TCACAGGATC CTGCCTCCCT GGCCAGGAGC TCAGGCTGGT 60 TTGGAACCAT ATGGAAGGAG GCAGCTCAGG AAGACTGGCA GCAGGGAGAG GTAAGCAACA 120 CTCAGGGAGG ACACAGAGAT GTCAGCATTT CCAAAGAAGT CGGAAGCTCC CCTTTGCTCT 180 TCTCACAAAT AAGTTTCCCA AGAAGGGGCA GATGGGGCGG ATGGTTCTTA GGACACAAGG 240 TCCCACCGAA CATCTGCAGC ATTGAAGTGA AAGGGGAAAA ATGACTTGGA AATGCCCCTT 300 CACTGCAAAG CAGCCAGTAC CGGAGGCCAC AGAGGAGGGT GGCCAGGGAC AGACAAAGTG 360 CCCAGTGCCA GCCCAGCCGA GAGGCGGCAC GTGGGGAGTT GGGAACTTAC TGTGCTGGGC 420 CTGGGCAGGG ACCACCGGCC AGGGCTGCTT TTCCCTTCCA GAAACAGCTC CTCCTACGTT 480 TCGCTCCTTC CCCTGCTTTA GTCAAGCACA CCCCTCTTCG TGTTAATGTC TCGGCAGCTC 540 TGGGCATAAA GGAGGCAGCT GGAATAGCCC ACCAGGTGGG AGAGCCTGGT GAGTGTGGGA 600 GTCCCCAGAA CCACAGCCAG GAGCAGCTGG CAGGTGTGCC CGGCCCCACG GTGAGCACGC 660 AGGCATGGAG CTCACAGGAC AATGTCCGCC CGGGGCTGAG GGCCAGCCTG CCGAGGGCCA 720 GCCTGCCAAG GGCCTGAGGG ACAGGAACAA GAACAGCGCT CTCCGGGAGA GCCTTCTGAC 780 CAGGAAGCTG AGTGGCTGTG CCTTCCTGGG GACTAGCCAC TAGGGAGAAC CGCCTCTCAA 840 AAGTTCCCCC AGGAAAAACA AAACCTACTT CGAGCTGCTG GGAGGGCAGG TTACTCACCT 900 CTGTATCCCA GGTAACAGAT GCCTGATGCC CACTGGCCTT CCTCCCTCCC TCTTTCCTTC 960 CTCTCCCCCA ACCCCATTCT CTCCTTTACC ACTTCCTTCC TTAGTTCATT TTTGCTCCAC 1020 TTCATTCCAA ATAGAATTTG AGATGACTCA TCGAATGAAT TCAACATAAC TAAATAAAAT 1080 TTTTAAAATA AAAACCAAAC CAATAAACAA GCACAAAAAC AGGGTTAAAG ACAAGAGTGG 1140 CCAGGCCAGA GAGAAGGAAA GGTATGCAGC GAAACCTCAG TTATGGGAAT GAGGCACCAG 1200 ACGGTTCTGA GTTACAAAAC GGGAGATGGA GGCCGGATAC ACGGCAGATC TTGGTGACAT 1260 AGAGTCCCGG ACCTGCCCGA GGCGGGTTTA TTTCCTCACT TAGCACTCAG AGCTAAGAGG 1320 AAGGGTGGCC AGCCCGGGCC ACATCGTGTC CTCAGCTGTT AGACTCACCC AGGCAGCTGT 1380 TTAAACTGAT CTCACTGATC TCATGACTAC ATGGTCAGTC ACGTCCCTTT AACTGACAGG 1440 GAGATTTGTG TGTGCTTTTT TGTAACATCT TACATGCACT TACATTCTTT TATTTTTATC 1500 ACTTATTTCA TAACGAAAAC ATTTCTTCAC ATAGAAAAGT GGACCAAGGG AGGGGAGGTG 1560 GGGAGGGCCT CATTGGGCCC CCAGCATAAC CCTATCAGTG GGCAGGGTGT TCTGGGGGCG 1620 CCCATTCCAC TGGAAACCAC GTGGTGTCTC CTTCCAGGCT GAACACAAAC AGGGGGCCCC 1680 AGTTTATAAC TAGCCAGGGG TGCACTGCTC AGACCAGGCT CAGCTCCACA AGGCAGCCTG 1740 CGCTTCCTGC CACCTGCCCA CCATTTGGCA GGGGCAGACA CAGCAGTGAC GGCAGGGGGT 1800 CAAAATAGGA CCACCTGTCC CTTTACTGGC CACAGTCATC AGACCCGGAG ACACTAAACA 1860 GGACTTTAAC TCCTCCGAGC ATTGGTTTCC ACCTCTGTGA AACTAGCTGA CAACACCACC 1920 AGCCTCCCAG GATCTCTGTG GGGACTAAGA AGATGCCTCA AGGCACCAAG CCCAAGCCAG 1980 CAGCACTCAT CATCAGCCCT GGGGGAGAGA GGAGGGTTGC ATGTGTTGTT TCCAGTCCAA 2040 CTCCCGCATT TTACAATGGA GGAAAGGCCA TGGGGAGGGG CTGCTCTGGG GGGGCAACAG 2100 CTGGGCAGGG TGTGGCACCC TGAGGACAGG CCAGTTTATT CCTTACTTCA TGGTGACAGA 2160 AAACAGGCCG AGCCCTAGAG AGCCAGCTCT CTCAAAGTAC CCCCAATGGG AGTGTCCTCA 2220 ACTGCAGGCA GCGGCCAGCC AGGCAGAGCC AGGCAGGGGG CTCCCATCCA TAGGCGAGCA 2280 AGTTAGCAAG GGCGGCCTGG GAGGGAAGTG CCTTCTCTAG AAGGTGACAA CATTGTTAAT 2340 GAGCCCGTGT TAATGTCAGT CATCTCCGGA GTCTGAAAGT GCCCTGCAGC AGGTGGGAGG 2400 GGTTATGTAT GCTGAGTCCA CTCTGGAGTA TGCCCTGCAG AGCTGCGTTC TGTCCTGTTA 2460 GATGTCCCAC 2470
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