Tag | Content |
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EnhancerAtlas ID | HS099-10647 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr18:77549370-77552530 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr18:77550896-77550914 | CCTTCCTTCCCTCCCTCC | - | 8.45 | EWSR1-FLI1 | MA0149.1 | chr18:77550880-77550898 | GCTTCCTTCCCTCCTTCC | - | 8.91 | EWSR1-FLI1 | MA0149.1 | chr18:77550884-77550902 | CCTTCCCTCCTTCCTTCC | - | 9.09 | EWSR1-FLI1 | MA0149.1 | chr18:77550892-77550910 | CCTTCCTTCCTTCCCTCC | - | 9.47 | EWSR1-FLI1 | MA0149.1 | chr18:77550888-77550906 | CCCTCCTTCCTTCCTTCC | - | 9.72 | Myog | MA0500.1 | chr18:77552361-77552372 | GACAGCTGCAG | + | 6.62 | RELA | MA0107.1 | chr18:77549832-77549842 | GGAAATTCCC | - | 6.02 | Tcf12 | MA0521.1 | chr18:77552361-77552372 | GACAGCTGCAG | + | 6.14 | ZEB1 | MA0103.3 | chr18:77550046-77550057 | GGGCAGGTGCG | - | 6.02 | ZNF263 | MA0528.1 | chr18:77550980-77551001 | TCTCCCTCCCTCTCATTCTCT | - | 6.01 | ZNF263 | MA0528.1 | chr18:77550941-77550962 | CCCCCCTTCTCTCCCTCTCTC | - | 6.18 | ZNF263 | MA0528.1 | chr18:77550921-77550942 | CTCTCTCTCCCTCCCTGCCCC | - | 6.33 | ZNF263 | MA0528.1 | chr18:77550949-77550970 | CTCTCCCTCTCTCTCTCCCTC | - | 6.34 | ZNF263 | MA0528.1 | chr18:77550913-77550934 | CCTCTCTCCTCTCTCTCCCTC | - | 6.35 | ZNF263 | MA0528.1 | chr18:77550880-77550901 | GCTTCCTTCCCTCCTTCCTTC | - | 6.53 | ZNF263 | MA0528.1 | chr18:77550888-77550909 | CCCTCCTTCCTTCCTTCCCTC | - | 6.5 | ZNF263 | MA0528.1 | chr18:77550884-77550905 | CCTTCCCTCCTTCCTTCCTTC | - | 6.67 | ZNF263 | MA0528.1 | chr18:77550904-77550925 | CCCTCCCTCCCTCTCTCCTCT | - | 7.17 | ZNF263 | MA0528.1 | chr18:77550892-77550913 | CCTTCCTTCCTTCCCTCCCTC | - | 7.27 | ZNF263 | MA0528.1 | chr18:77550896-77550917 | CCTTCCTTCCCTCCCTCCCTC | - | 7.95 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr18 | 77551694 | 77552094 | chr18 | 77550515 | 77551000 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I079790 | chr18 | 77550351 | 77553372 |
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Enhancer Sequence | CACACACGTG CACACACGCA CTCTCACACG TGCACGCCTG CACACTCGCA CACTCAAGCA 60 CACTTGCACA CGCACTCCCA TCTCACAGAC CTGGGCACAC AGGCACATAC GGGTGTGAGT 120 CAGCAGCACG GGTGGGCTCA CCACAGAATC TGAGCGAGGC ACCTCCCACG GAACCTCCGT 180 GCCCTCCCAG GATGGAAACC CCACGGCTCC GCTGCTCCCA GGGGGCCCCG CATGCCCCCC 240 GCCGCGGGGG CAAGACGTGA ACAGGCCAAG CACTGCCCTG AGCGGCACAG GAGGCCCTGG 300 AGCCCGGCCG GCTCAGGCTC CCCGCAAGGA AAGCAGCCCA TCCACGGACC AGGCCTTAGA 360 GCCACGGGCG CACAGCGCGG TGCACACGCG AGAGGCAGAA TGAGGAACGG GCTCGCGGGC 420 TGGACGCTGG CGGGGACAGG AGCCTCCACA GGGGCCGCTG CGGGAAATTC CCGGGCCCCA 480 GGCTTTTTGC GCAGGGACCT CGTCTTGTCC TTGGTATTCC AGAGGCCATG ACCAGACTCT 540 AGTCTCATAA GAAGTACAGA AATTCCTAAA TTGCTCAGAG GTGCCTCCTG TGCCAAGGAA 600 GGGGACGTCC GTGCCCCTCC TTGTCCCGGG GAGCACGGCT CCATGGCGCC CGCTGTGGAG 660 CTGCGGTTCT CACCATGGGC AGGTGCGAGG CCGTAGACTG GTGTGGTCAG ACCAGGGGAC 720 TCCTGCGTTC ACCCTGGGCC CCGGAGACTA GTGATCCCGC TCCCCAGCAG AGCACCGCCA 780 AAAGCCCCGG GTGCCGGAGC TGTCCTGCAA GAATGAACGG GCAGGAGACA CAAGAGCGTG 840 GCGGGGCCTT CCGAGGATGC GGTGCAAGGG CGCTGTTAGC ACCCACGCGA GGCGGCAGCG 900 CATGGAGGAA GCCTCCCATC GTAAGCGCGT TTCTGCCTGA AATGCACGTG TCCTTATAGG 960 CAGCGGTCTT GCCACTCATG GACGGAGAGG CAGCATATGT TTAAAAGATG AGCACACAAA 1020 GGACTGTGCA CCTGCCGCGG AGTGGCGTCC TCTGGGAGAA GCTGGAGAGT TTGAAGGGGT 1080 GGACAGGAGG CGGGAGACAG GGGAAGACGG AGCTCAGACC TGTAGGGGCT GCTGTGCTGG 1140 CCCAGAGTGT CCAGGGTTTG GGAGTGGAGG AAGGAGGCAA GTCTTTTCCA GTTAGGGAGA 1200 AACCACACAG ACCCTGAAAC CCGGTCCCCA CATGCAGACC CAAAACCCAG TCCCATCCCA 1260 GGAGGCTGGG CCACCACCGT TGTGGGTGCT GAGTCCCTTA CTTTCTGCCT CACCCGTTCC 1320 ACTGAGCCTC TTTCGCGCCA CCCTCACTGT CATTTGCAGG AAACACCTGT TCTCTCCATG 1380 CACCTGCTCT GATGCACTGA CTTGTTACCG GGAAGGTGGC TGCTTCCAAG GCAGGCCAAG 1440 ATGCCTGCGG CTTGTTATTC GTCTGAGAAT GGCTCCTTGC TCTAACGGGG TTTGAGGGAC 1500 AGACGGGACT GCTTCCTTCC CTCCTTCCTT CCTTCCCTCC CTCCCTCTCT CCTCTCTCTC 1560 CCTCCCTGCC CCCCCCCTTC TCTCCCTCTC TCTCTCCCTC TCTGGTTTTC TCTCCCTCCC 1620 TCTCATTCTC TCTAGCACTT TCTCCCTCCA TTCTCCCTCT GATTCTCCCT CTTTCTCAGT 1680 GCTGCCTCCT GCCTCTATGA TCTGAACAAA TTTTCTGTGG AGATCGAAGT TGGTAGGGGG 1740 CAGGGGGTGG CAGCCTGTGT TTTTGGTAGA ATTTCAAGCA CGTTTTACAG GAGGAGCTGA 1800 CACTGTCGGG CCATTATCTT TCCTGAGCAA TGACAGCAGC ACCTCCTGGC CTTGGGTCTT 1860 ATCATCATAT TGTTCCCGAG TGTGGCTTTC AATGCAGCTA ATTACATAGG TTGTTGTTTT 1920 CTTCCACAGA GTTTTCCAGC CTCTCCAGGG CAGAGGCTGT GTCTGGTGAA TGTCCAGGCA 1980 CTGCAGCGCC TGGCACACGG CACTGGGTAG GTGCTTAACA CAACATGTGA ACAAATATTT 2040 ATTGAACTAC ATAAAGGTAA ACCACTCCAT TCACAGAAGA GAAATATCTC TGTTGAGAAT 2100 GTCATGGATG CCACGTAATT GGGGAGCAAA AGGAAGCCCC AGTCACCCAC AACCTTTCAC 2160 AGCACACGGT GCAGGGCTGG ACAGTGCAAA TAACTTACAG GGGTTTCCTC ATCAAATCCA 2220 AGGCCATTTC CCAGAACTGT GACAGTAGTG AAATGGAATG TTACATTCAC AGCACAAAAT 2280 TGACAGAGAC AGAAAGGACG TCTGCATTCC ACTGTGGGTT TAAATGAAAC GGTGAGATGC 2340 TCGGAGGAAG CGCCGGCTGC TTGCTGCATC AGGAACGTTT CGTAATAGCA AAGGCACTAT 2400 CGGGAAGCGT TACGTAAGCT GTCCATTAAG GACACTGATT AGGAACGTTC AGAAATATGA 2460 AAACCGCATA GCATTGTTTG CTGGCCTCAA CCACATGCAG CTTGCTTTCA GCAAGAGGGA 2520 AGGAAGTGAT CACAGAAGGT GCAGGTCACT GCTGGGATGC CCCCTGGGCT GAGATAACTG 2580 AACGTATGAA ACTGCTCCCT TGCCAACAGC TCGGTAAGAA CGCAAGTGCT CGCGTTACAA 2640 AAGAATTTGG CATGAAGAGC TGTTCGTCAG AGAGCCCACC AGAGTCGTGT ATACGTTTGA 2700 ATCCACTTCC AACGTTTTAA TTTACACAAA TTTCAGGAGC ACACTATTAG CCGAGTGGAA 2760 GGTGGTCTTA TCCTCTGCAC CACACGTGGG TCCGAGACCC CAGAGCACAG TCGTCTCCCT 2820 CGCCAAGAAT GCACTCGGCA GCCAGGGACT CGCAGAGTGA ACGTGTGCGG GTTTCAGTGG 2880 ACCGCTTCCC ATCTGGAGCT CAAGTTAAGA TGAGGAAGTA GAATCACAGT AAATGAGGAG 2940 TTAGGGAATT TAGGGTAGAG ATTAAAGTAA TGAACAGAGG AGGAGGCCTG AGACAGCTGC 3000 AGAGAGACCC TGTGTTCCCT GTGAGGTGAA GCGTCTGCTG TCAAAGCCGG TTGGCGCTGA 3060 GAAGAGGTAC CGGGGGCAGC ACCCGCCTCC TGGGAGAGGG ATGGGCCTGC GGGCACCTGG 3120 GGGAACCGCA CGGACACAGA CGACACTATA AACGCGGGCG 3160
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