Tag | Content |
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EnhancerAtlas ID | HS052-28406 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr4:38753070-38755460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr4:38754111-38754122 | AGTGACTCATC | + | 6.02 | JUND | MA0491.1 | chr4:38754111-38754122 | AGTGACTCATC | + | 6.32 | Klf1 | MA0493.1 | chr4:38753511-38753522 | AGCCACACCCT | + | 6.02 | ZNF263 | MA0528.1 | chr4:38754775-38754796 | GGGGGTGGAGGGTGGGGAAGG | + | 6.35 | ZNF263 | MA0528.1 | chr4:38754778-38754799 | GGTGGAGGGTGGGGAAGGGGC | + | 6.3 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 38753338 | 38753545 | chr4 | 38753943 | 38755431 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I038752 | chr4 | 38753622 | 38755951 |
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Enhancer Sequence | CAGACAAGGA GACAAGCAGA GGAATGTCAA AATGCTGCGG CAGAAAGAGA GAAGAGGAGG 60 AATGTCTCAA CACTAAGAGT TTAGCCCGGG GCGGTTCAGC TGCCGGAAGG CCAAACTCCA 120 GGAGAAGCCC ATCTTCCTAC TCCGTCCTCC CTTCAGGTTC TCCATCCATC CTGCTGAGAG 180 CCACCTCCGC CATTCAGTAA GACCCCCACA TTTATCCTTC AAGTGCATGT GTGACCCAGT 240 TCTTCCAGGA TGCTGGACAA GAGCTTGGGA TACATAAAGC TGTCACACTG GCCCTCTGCC 300 CTTGCTCGCT AACACTCAAG CCATTCGCAG ACGGCTAAAA GAGCACATTG TAACACGTGC 360 CCACTTGGAC TCCTGCACCT GCCCATCTGC ATGCTTTCCA TCCTGTAAGG GGTTTGAGTG 420 GTGTCAGCAA TCTAACAGAC AAGCCACACC CTTGTTTCAC GTCCTGTGAG AGGGGTCAGG 480 GAACTCTTCT GTTTCATCAT TACCCAACTT TGGAACTCAA GAAAGGACTC ACAGGGAAAT 540 TCTTGCAGAA TCTCGTGGAA AATCTCACAT GTATTTGTGA AAATACAATG TGGATCTGTG 600 AGATCCCACT TCAACACAGG CCACGGGGCC ACCTTCTGCA CCCACATGGG TTGTTTTAAG 660 TCTTCCTTAG TCTCCTTGAG AATAACATGA TGCTATGATG TTGGCAGGAA TCTTCCACAC 720 CTTCCAAAAC ATGACAATAT GGGTCAAGCC CGTGCAGAGA CTGTGGCTCC TGCTTTGGGA 780 GTCACCTGGA ATTGTTGAGA GATTAGCAAA TCCCAGAACC AGGTTTGTTA GAATTAACTG 840 CTCAACCAGA TTGTATTGAA AATGGTCTGA AGTCAAAGAC GACAGACGCA AACGGGCTAA 900 ATTGCTCAGT TAATTCTTCC ATTTCTCTTC CTCCTAGTTG TTCTAGCTTC AGGGAGGACT 960 CAGGAGAGTA CTGTTTGAAA ACCACTGATC TAGTTTACAC TTTCATTTTA CAGAGAGGAA 1020 ACTGAGAGCC ACAGAGATTC AAGTGACTCA TCCAAGATGA CCCAAACCCT GGGGTTTGTT 1080 ATTGTTTTTC ACACTATGCA AAGCACTAAA AAACATTCGT TTGAAACAGG TGAACAAAAG 1140 TCTAATTTGT AGTGAGGTCT AGGGGAATGA CTGTCCAGTC AATTCCTCAA TTCATGAAGG 1200 AGCATTTGGG ACGCCACAGA GGAACATACA CAGGTATCCC TCCTCCTACC CGACACCATT 1260 CAGGAAGAGC GGTTACCCCT CCAATGCACT GAAGCAGATT CATTTCCCTC AGGACTGTGG 1320 GAGGCGACTG AGGCTGAGTG AATGATACAG CCTTTTAATT TGTTTTTAAT TGTCGTGTCC 1380 TGGTAACCCT TCCAAAGACC CTTCACGGAG AGTAGTTTTA TTTTTCCACT TATTAACCGC 1440 ATTCACTAGA CTGGAAAAAG AATTCCCTAT CTCCCAAGAA CTCTCCCTTT CATTCTTGTA 1500 ATTCCTTTTT TTTTTTTTTT TTTTTTAGCA CCAGGAAAGT AATGTGTGTA AAACTAGAGC 1560 CAAGTATATT GTGGTTTCAA ATACAAGCCT GTTTGGAGCA GAAGCCCGTG GGATTGCTGC 1620 GTTTCAGCCT CAGGGGATGG CCCGCTGATG GCCTCGGCCT GTGAAAGGGA GGGGCTTGAA 1680 TGGCCCTTTG ATTCAGCCCA AATCTGGGGG TGGAGGGTGG GGAAGGGGCA GGCCTGTTAT 1740 TTGACACTTT CTGTTGGGCT TGGCCCAGGC CTCACTCCTT ATGCAGGCCT CCCTGGAGCC 1800 TGCAAGCCCT CTCTGAGGAC GCACTGACTT AGCAAGCGCT GAAATGCATA ACATTCCTTG 1860 CTGCTTAGGA AGTAGACCAG CGATCCCCAG GGCTCGCGAA TTCCCTGCGC TTTGAGAATG 1920 GTGCTCTTTA TAACGTTCCC CATCCAAACA CACACACAGA CACGCTACAC ACACATACCC 1980 CAAACATACA CACACACGCG CACACACACT CCACACACAC CCAAACATAC ACGTACACAC 2040 ACACTCCACA CACACACACC CCAATATACA TACACATGCA CACAATAGAC ACACACCCAA 2100 ACATGCACAC ACACTCCACA CACACACACC CAAATAAACA CACACATGCG CAAACTACAC 2160 ACACATTACA CACACACCCA TACACACACA TCCAAAAATA CACACACACA AACTACACAC 2220 ATACTACACA CACACACAAA CATACACACA CGTGCACACA CACGCTCCAC ACACACATCC 2280 CAACATACAC TCTACACACA CGCCACACAC ACCCCATACA CACAGGCACA CAATCCACAC 2340 ATACACTCCA CATACACAAA CCCAAAACAT ACATACTCTA CACACACACC 2390
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