Tag | Content |
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EnhancerAtlas ID | HS197-19536 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr7:47491500-47495210 |
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 | CACTCTTTGT AATACTAATG CCTGGGTAGG CAGCCAGCTC TACTGCTCGA GTAAGCCGTC 60 TGATCTTGGG AATTTACTTG CCCTCTGTGT GACTCAGTTT TCTCATCTGG AAAAGGGAGA 120 CAGAAACAGC ATTCTTGGAA GGATTAAATA AGGAAACATA AACATAGGGC TTAGAACAGT 180 GCCTGGCCAG TAATAAGTGC CAAAGAAATA TTAGCTACTT ATTCCATCAT CTTATTTCTG 240 TGTCAGGCCT CTGTGAGGCC CTGGAAATGC ACTTTATCCA CAAGTTATTA GGATCCCCCT 300 TAGATCACAA AACCAGCTGT GACCACAATG CCCATTTAAC AGTAGGAGAA ACAATGCTCA 360 GAGAGGGTAA GTGATTTTCC CAAAGCCACA CAGTTAATAA GACATTTTTT TCCCTTCCAG 420 AACAAGAATA CCAGGAACCA ATTAATTGTC AGGATTGCCC AACTTGATTT TCTGCTTAAT 480 GCTTTTAAAC ATAAGCAGCA ATCGTTAAGA ACTGCCAGAG AAAGTACACC CCATGGAGGG 540 TGGGAAACTA AAATAAAGTC ATCTTGTCAT TTTACCTTCA TGTTCAACTA TGAGAAACAA 600 CAGACTAAGA TTGTATCTCT ATTTATTTGT AACGAAATAG TCACAGGATC CTGCCTCCCT 660 GGCCAGGAGC TCAGGCTGGT TTGGAACCAT ATGGAAGGAG GCAGCTCAGG AAGACTGGCA 720 GCAGGGAGAG GTAAGCAACA CTCAGGGAGG ACACAGAGAT GTCAGCATTT CCAAAGAAGT 780 CGGAAGCTCC CCTTTGCTCT TCTCACAAAT AAGTTTCCCA AGAAGGGGCA GATGGGGCGG 840 ATGGTTCTTA GGACACAAGG TCCCACCGAA CATCTGCAGC ATTGAAGTGA AAGGGGAAAA 900 ATGACTTGGA AATGCCCCTT CACTGCAAAG CAGCCAGTAC CGGAGGCCAC AGAGGAGGGT 960 GGCCAGGGAC AGACAAAGTG CCCAGTGCCA GCCCAGCCGA GAGGCGGCAC GTGGGGAGTT 1020 GGGAACTTAC TGTGCTGGGC CTGGGCAGGG ACCACCGGCC AGGGCTGCTT TTCCCTTCCA 1080 GAAACAGCTC CTCCTACGTT TCGCTCCTTC CCCTGCTTTA GTCAAGCACA CCCCTCTTCG 1140 TGTTAATGTC TCGGCAGCTC TGGGCATAAA GGAGGCAGCT GGAATAGCCC ACCAGGTGGG 1200 AGAGCCTGGT GAGTGTGGGA GTCCCCAGAA CCACAGCCAG GAGCAGCTGG CAGGTGTGCC 1260 CGGCCCCACG GTGAGCACGC AGGCATGGAG CTCACAGGAC AATGTCCGCC CGGGGCTGAG 1320 GGCCAGCCTG CCGAGGGCCA GCCTGCCAAG GGCCTGAGGG ACAGGAACAA GAACAGCGCT 1380 CTCCGGGAGA GCCTTCTGAC CAGGAAGCTG AGTGGCTGTG CCTTCCTGGG GACTAGCCAC 1440 TAGGGAGAAC CGCCTCTCAA AAGTTCCCCC AGGAAAAACA AAACCTACTT CGAGCTGCTG 1500 GGAGGGCAGG TTACTCACCT CTGTATCCCA GGTAACAGAT GCCTGATGCC CACTGGCCTT 1560 CCTCCCTCCC TCTTTCCTTC CTCTCCCCCA ACCCCATTCT CTCCTTTACC ACTTCCTTCC 1620 TTAGTTCATT TTTGCTCCAC TTCATTCCAA ATAGAATTTG AGATGACTCA TCGAATGAAT 1680 TCAACATAAC TAAATAAAAT TTTTAAAATA AAAACCAAAC CAATAAACAA GCACAAAAAC 1740 AGGGTTAAAG ACAAGAGTGG CCAGGCCAGA GAGAAGGAAA GGTATGCAGC GAAACCTCAG 1800 TTATGGGAAT GAGGCACCAG ACGGTTCTGA GTTACAAAAC GGGAGATGGA GGCCGGATAC 1860 ACGGCAGATC TTGGTGACAT AGAGTCCCGG ACCTGCCCGA GGCGGGTTTA TTTCCTCACT 1920 TAGCACTCAG AGCTAAGAGG AAGGGTGGCC AGCCCGGGCC ACATCGTGTC CTCAGCTGTT 1980 AGACTCACCC AGGCAGCTGT TTAAACTGAT CTCACTGATC TCATGACTAC ATGGTCAGTC 2040 ACGTCCCTTT AACTGACAGG GAGATTTGTG TGTGCTTTTT TGTAACATCT TACATGCACT 2100 TACATTCTTT TATTTTTATC ACTTATTTCA TAACGAAAAC ATTTCTTCAC ATAGAAAAGT 2160 GGACCAAGGG AGGGGAGGTG GGGAGGGCCT CATTGGGCCC CCAGCATAAC CCTATCAGTG 2220 GGCAGGGTGT TCTGGGGGCG CCCATTCCAC TGGAAACCAC GTGGTGTCTC CTTCCAGGCT 2280 GAACACAAAC AGGGGGCCCC AGTTTATAAC TAGCCAGGGG TGCACTGCTC AGACCAGGCT 2340 CAGCTCCACA AGGCAGCCTG CGCTTCCTGC CACCTGCCCA CCATTTGGCA GGGGCAGACA 2400 CAGCAGTGAC GGCAGGGGGT CAAAATAGGA CCACCTGTCC CTTTACTGGC CACAGTCATC 2460 AGACCCGGAG ACACTAAACA GGACTTTAAC TCCTCCGAGC ATTGGTTTCC ACCTCTGTGA 2520 AACTAGCTGA CAACACCACC AGCCTCCCAG GATCTCTGTG GGGACTAAGA AGATGCCTCA 2580 AGGCACCAAG CCCAAGCCAG CAGCACTCAT CATCAGCCCT GGGGGAGAGA GGAGGGTTGC 2640 ATGTGTTGTT TCCAGTCCAA CTCCCGCATT TTACAATGGA GGAAAGGCCA TGGGGAGGGG 2700 CTGCTCTGGG GGGGCAACAG CTGGGCAGGG TGTGGCACCC TGAGGACAGG CCAGTTTATT 2760 CCTTACTTCA TGGTGACAGA AAACAGGCCG AGCCCTAGAG AGCCAGCTCT CTCAAAGTAC 2820 CCCCAATGGG AGTGTCCTCA ACTGCAGGCA GCGGCCAGCC AGGCAGAGCC AGGCAGGGGG 2880 CTCCCATCCA TAGGCGAGCA AGTTAGCAAG GGCGGCCTGG GAGGGAAGTG CCTTCTCTAG 2940 AAGGTGACAA CATTGTTAAT GAGCCCGTGT TAATGTCAGT CATCTCCGGA GTCTGAAAGT 3000 GCCCTGCAGC AGGTGGGAGG GGTTATGTAT GCTGAGTCCA CTCTGGAGTA TGCCCTGCAG 3060 AGCTGCGTTC TGTCCTGTTA GATGTCCCAC CCAAACTCAC ACAGATCCCC CTGCAGAGAG 3120 CCTGGAAACC AGCCCCTCAG GGCACAGCAC AGGCATCCCA AGGACAGCCC CACCAAACCC 3180 CCAGCATACA GATACCTGGT CCTGTCCACA TGGGATGTCG GGGGTGCTGA CGGGGGCAAG 3240 ACCCACAGAT GCTGACCACC ATGGGCCACA GAGATAGGTC TCTGGCCCTG CAGCCAGCTG 3300 GTTCCATACA ATAGCTCAAT GTTTGCAAGG CTGAGGGAAG GGCCTAATTC ACCCACCCCA 3360 GCCTGGCCAA CTCTGATGGG CAAAGGGGCT GCCCAGAGAA TGCTGAGAGG ATCACCCCAA 3420 CTCAGACCAG GACCATACCT GCCTCCACAC CCAGAAGGGC ACAGCAGGGC TTTTGCTTTA 3480 GAATGAAGAG CTAATGAATT GCACTGACAC TGACAGAGCA GCCTTAACCT GGAGTTTATC 3540 CCACAATAAT CAGATTCATA TGGATAACCC TGGAAACAAC AAGCAGAGAG GGCTCTGAGC 3600 AGCCCTGCTT CCCTTTCATA TCCACAAATG CAAACAAGTA TTTGCAGGAG GGCTAGCCCA 3660 TTTCAGGCAC TGCAGGGAGA ATGCAGGTGT GACAGAGGGG AAAGACCAGG 3710
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