Tag | Content |
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EnhancerAtlas ID | HS091-22612 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr18:77549820-77553050 |
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: 3 | Chromosome | Start | End |
chr18 | 77551694 | 77552094 | chr18 | 77550515 | 77551000 | chr18 | 77552400 | 77552575 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I079790 | chr18 | 77550351 | 77553372 |
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Enhancer Sequence | GGGGCCGCTG CGGGAAATTC CCGGGCCCCA GGCTTTTTGC GCAGGGACCT CGTCTTGTCC 60 TTGGTATTCC AGAGGCCATG ACCAGACTCT AGTCTCATAA GAAGTACAGA AATTCCTAAA 120 TTGCTCAGAG GTGCCTCCTG TGCCAAGGAA GGGGACGTCC GTGCCCCTCC TTGTCCCGGG 180 GAGCACGGCT CCATGGCGCC CGCTGTGGAG CTGCGGTTCT CACCATGGGC AGGTGCGAGG 240 CCGTAGACTG GTGTGGTCAG ACCAGGGGAC TCCTGCGTTC ACCCTGGGCC CCGGAGACTA 300 GTGATCCCGC TCCCCAGCAG AGCACCGCCA AAAGCCCCGG GTGCCGGAGC TGTCCTGCAA 360 GAATGAACGG GCAGGAGACA CAAGAGCGTG GCGGGGCCTT CCGAGGATGC GGTGCAAGGG 420 CGCTGTTAGC ACCCACGCGA GGCGGCAGCG CATGGAGGAA GCCTCCCATC GTAAGCGCGT 480 TTCTGCCTGA AATGCACGTG TCCTTATAGG CAGCGGTCTT GCCACTCATG GACGGAGAGG 540 CAGCATATGT TTAAAAGATG AGCACACAAA GGACTGTGCA CCTGCCGCGG AGTGGCGTCC 600 TCTGGGAGAA GCTGGAGAGT TTGAAGGGGT GGACAGGAGG CGGGAGACAG GGGAAGACGG 660 AGCTCAGACC TGTAGGGGCT GCTGTGCTGG CCCAGAGTGT CCAGGGTTTG GGAGTGGAGG 720 AAGGAGGCAA GTCTTTTCCA GTTAGGGAGA AACCACACAG ACCCTGAAAC CCGGTCCCCA 780 CATGCAGACC CAAAACCCAG TCCCATCCCA GGAGGCTGGG CCACCACCGT TGTGGGTGCT 840 GAGTCCCTTA CTTTCTGCCT CACCCGTTCC ACTGAGCCTC TTTCGCGCCA CCCTCACTGT 900 CATTTGCAGG AAACACCTGT TCTCTCCATG CACCTGCTCT GATGCACTGA CTTGTTACCG 960 GGAAGGTGGC TGCTTCCAAG GCAGGCCAAG ATGCCTGCGG CTTGTTATTC GTCTGAGAAT 1020 GGCTCCTTGC TCTAACGGGG TTTGAGGGAC AGACGGGACT GCTTCCTTCC CTCCTTCCTT 1080 CCTTCCCTCC CTCCCTCTCT CCTCTCTCTC CCTCCCTGCC CCCCCCCTTC TCTCCCTCTC 1140 TCTCTCCCTC TCTGGTTTTC TCTCCCTCCC TCTCATTCTC TCTAGCACTT TCTCCCTCCA 1200 TTCTCCCTCT GATTCTCCCT CTTTCTCAGT GCTGCCTCCT GCCTCTATGA TCTGAACAAA 1260 TTTTCTGTGG AGATCGAAGT TGGTAGGGGG CAGGGGGTGG CAGCCTGTGT TTTTGGTAGA 1320 ATTTCAAGCA CGTTTTACAG GAGGAGCTGA CACTGTCGGG CCATTATCTT TCCTGAGCAA 1380 TGACAGCAGC ACCTCCTGGC CTTGGGTCTT ATCATCATAT TGTTCCCGAG TGTGGCTTTC 1440 AATGCAGCTA ATTACATAGG TTGTTGTTTT CTTCCACAGA GTTTTCCAGC CTCTCCAGGG 1500 CAGAGGCTGT GTCTGGTGAA TGTCCAGGCA CTGCAGCGCC TGGCACACGG CACTGGGTAG 1560 GTGCTTAACA CAACATGTGA ACAAATATTT ATTGAACTAC ATAAAGGTAA ACCACTCCAT 1620 TCACAGAAGA GAAATATCTC TGTTGAGAAT GTCATGGATG CCACGTAATT GGGGAGCAAA 1680 AGGAAGCCCC AGTCACCCAC AACCTTTCAC AGCACACGGT GCAGGGCTGG ACAGTGCAAA 1740 TAACTTACAG GGGTTTCCTC ATCAAATCCA AGGCCATTTC CCAGAACTGT GACAGTAGTG 1800 AAATGGAATG TTACATTCAC AGCACAAAAT TGACAGAGAC AGAAAGGACG TCTGCATTCC 1860 ACTGTGGGTT TAAATGAAAC GGTGAGATGC TCGGAGGAAG CGCCGGCTGC TTGCTGCATC 1920 AGGAACGTTT CGTAATAGCA AAGGCACTAT CGGGAAGCGT TACGTAAGCT GTCCATTAAG 1980 GACACTGATT AGGAACGTTC AGAAATATGA AAACCGCATA GCATTGTTTG CTGGCCTCAA 2040 CCACATGCAG CTTGCTTTCA GCAAGAGGGA AGGAAGTGAT CACAGAAGGT GCAGGTCACT 2100 GCTGGGATGC CCCCTGGGCT GAGATAACTG AACGTATGAA ACTGCTCCCT TGCCAACAGC 2160 TCGGTAAGAA CGCAAGTGCT CGCGTTACAA AAGAATTTGG CATGAAGAGC TGTTCGTCAG 2220 AGAGCCCACC AGAGTCGTGT ATACGTTTGA ATCCACTTCC AACGTTTTAA TTTACACAAA 2280 TTTCAGGAGC ACACTATTAG CCGAGTGGAA GGTGGTCTTA TCCTCTGCAC CACACGTGGG 2340 TCCGAGACCC CAGAGCACAG TCGTCTCCCT CGCCAAGAAT GCACTCGGCA GCCAGGGACT 2400 CGCAGAGTGA ACGTGTGCGG GTTTCAGTGG ACCGCTTCCC ATCTGGAGCT CAAGTTAAGA 2460 TGAGGAAGTA GAATCACAGT AAATGAGGAG TTAGGGAATT TAGGGTAGAG ATTAAAGTAA 2520 TGAACAGAGG AGGAGGCCTG AGACAGCTGC AGAGAGACCC TGTGTTCCCT GTGAGGTGAA 2580 GCGTCTGCTG TCAAAGCCGG TTGGCGCTGA GAAGAGGTAC CGGGGGCAGC ACCCGCCTCC 2640 TGGGAGAGGG ATGGGCCTGC GGGCACCTGG GGGAACCGCA CGGACACAGA CGACACTATA 2700 AACGCGGGCG AGACATCAGG GACCGGGAAA CAGAAGGACG CGCGTTTCGA GCAGCTGCCC 2760 AGTGGGCCAC AAGCCCCGCC ACGCCACAGC CTCTTCCCCT CAGCACGCAG AGAGGGAGGC 2820 TGCAGATGCC AGAAACGGGC CCCTGTCTCC CATGAACAAG AAACAGAAAA AAAGGAAGAG 2880 AGCAGAGAGC CAGGCAGATG TTCAGGAGAA TGAACGTGTC CGAAAGACAG ACAGAAGCCC 2940 GGGGACTGAC GTCCGTGGGA GCTCCTCCCG CACTGCAGAA GGTGAGTTCC TGGGTCCCCT 3000 CAGTACCACG CACGGGGAAG GCAGCGGGCG GAGGTCGGGA GGGCTGAGGG ACACAGGTTT 3060 CTCGGTGGGG TGGTGAAAAT GCTTTAAAAT GGATGTAGCA ACGGCTGCAC GCGCTGAATA 3120 AACTGAAAAC CACTGAATGG TGCAACTTAA ATGGGTGACT TGTATGGTGT CAATCCTATC 3180 TCGGAAAAGC TGCAGAATAT ATCATCTTAT TTTGAAAATC AGCCAAGATA 3230
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