Tag | Content |
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EnhancerAtlas ID | HS181-12567 |
Organism | Homo sapiens |
Tissue/cell | Sperm |
Coordinate | chr5:79401360-79402510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Esrra | MA0592.2 | chr5:79402109-79402120 | TTCAAGGTCAT | + | 6.62 | Esrrg | MA0643.1 | chr5:79402110-79402120 | TCAAGGTCAT | + | 6.02 |
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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 |
GH05I080105 | chr5 | 79401788 | 79402949 |
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Enhancer Sequence | GCCGCATCCT TAGCAACTAA GTTGGAAGAA ATGGGGCTCT TTGGCCAGCA ATGTCTTCCC 60 GCCATGGGCT ATACCTGCAG GTGCCGGGTG AGGAGGACTG CGGGCAGCTC TGAAGCCTCC 120 ACTTTTCCTT ATGGGTTTTT TGTTCACTCT CCAGGGCCTA ATTCAGATGT CACCTCCCCT 180 GTGCGGCTTC TCCAACCCTT CAGATAGATG TGATCACTCC CTCCCCTGAG CCCCAGAACA 240 CTTTGTCCAA TTTCCTGCAC CCTCTGAGAG CGTGGCACAG GCCCCCTCCA CTGTGTAACA 300 ACTCACAGCC CCTCCCTGCA TCAGAAGCCC ACCCCCTTCC TCCGGGGTGC CTCTTCTTTC 360 TAGTCATAGT GTCTTCCCTC AGTAGTCTAT CCCTCTGGGG ACTCTGAATA TCTTCCCTTC 420 CCCCTCAGCA ATCCCTAGCA CACTTGCAGC TGTGAGGGCT GCACCTGAGG ACAGAGCAGG 480 GGCGGGAACC CCAGTCTTAG AGGCTGTTGT CATCAAAGTT CAAATGGAAG ATCCTCTGAG 540 AAGGATCTGC AGGGAGACCA ATTGCCACCC CTAGGGAAGG CCGGGCTTCT GTGGTATCTC 600 AAGCCCTGGG ACCTAGAGGC AGCTTCCCGT AGGGAGCAGC CAGAAGGCCC TTTCCCTACC 660 CCCTCACCAC CCAGAGAGGC CTCCCTGGGA TGCCCTCCCC TGAACCCTAG AGCTTCATGG 720 GGATTGCTAT GTTTGCACTG TGATGTCATT TCAAGGTCAT GGTGATATGC GCTACAGCTG 780 AGCAAGATTG TTCCCAGCAT CAGATTGGAA GTTGAAAGAA AGGCTAAGTC ACAAGAACCC 840 AAGAGCTGGG TGAATGCACA GCTGTGCCCT AGGCCCACCA GCAAGGACCA CATTTATTAG 900 GCTCAGCCTC CCACACAAAC GGTGCCAGAA AGTCTAAGAG AAGAAGGGGA ACAGAGGAAG 960 GGAGGGAAAG TCCTTTAAAT CAACATGGTT TCATTGAGCT TCTGCACCAT GCAGGGGCCT 1020 GTGGGATTGA GAAGGAGAAT ATAATCCTAG TCCTTGCTCT CAGGAAGCTT ATCATCTGTG 1080 TAGAGCCCAA GAGTGAGCAG CTGGGTGAAC AAGAAGTGGT GCAAGGGGGA AGAGTTACCA 1140 CAGATGGTAT 1150
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