Tag | Content |
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EnhancerAtlas ID | HS181-01325 |
Organism | Homo sapiens |
Tissue/cell | Sperm |
Coordinate | chr1:236856020-236857490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PPARG | MA0066.1 | chr1:236857457-236857477 | GTAGGTCCCTGTGCCTCATT | + | 6.26 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_29956 | chr1:236849770-236856471 | Fetal_Muscle | SE_29956 | chr1:236856552-236857542 | Fetal_Muscle | SE_41020 | chr1:236848229-236857740 | Left_Ventricle | SE_51196 | chr1:236848318-236857838 | Skeletal_Muscle | SE_68016 | chr1:236801724-236870448 | TC32 |
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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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Enhancer Sequence | GATGTGTCCC GGGGTTGCCC TAGGCCTTCA GCCACATTCA CCAGGTAAGA AACTTAAGCC 60 CATTATAAGA TTTTCCAGAG TGTGGGAGGA GGAATATAAC TCTTAGCAGG GAAACTTAAT 120 TAACGCAGCC TCAGAAAACT GTCAGAAAGC ACCGCAGTCG GTTGCTGCAG CTGGGAGACA 180 CCTACAGAAA AGGCGCAGTT CTGGAGTGGG TGAGGGTGCT ACCATGATGA GCAGAGGAGT 240 TCACACGGAA TGCGTTGGAG GACAGTCAGA ATCCTACCGC CGTTTCCCTG GGAACGGCAC 300 TAAGTCTTCC AGAAAGAACA GAAAGCAGAG ATTGGGGGAG ACGCTTGCAA ACTACTATGC 360 TAGACAAATT TCAAAGGAAG GAAAACCTTA AGTGCAAGAA TTTGGCCTTT CTGAAGAAGA 420 CTGAGGAAAA TTTTTGGTAC AAACATCTGC ACACATGCAC ACACACACAC ACACACACAC 480 ACACACACAC ACACAGAGTT TTCTAGATTG GAAACTACAA GGTGTTTTTA CCTGCAACCC 540 TGGTGAGGAG CAAAATATAA ATGGAACACA AGCATGATGG TTCATTCTTT CATTCATTTG 600 GCAAACATTT TTGTAGTCCT AGGGACCAGC AGAGAGAGTT GATGACACCA CCATGGCCCT 660 TAAGGAGCTT ACAGCCAAGT TCAAGAGACA GGAGTGGTCT GTGAGAAGCA CAGAGGAGGG 720 GCATCTGCTT CAGCCAGGCT GGTGTAAGGA AGGTGTTTTC AAAGCCAAAG GTGTTTCAAA 780 CCCTCCTGCT TGGTTCCCCT TCATGGTGAA TGGAAATGTC TTTCTTCCAG GCGCCCAAGC 840 CAGAAACCCG AGTGTTACCC TTGCCCCCTC CTCCTCTCCC ACACCACGGC CGTTGGGTCA 900 CCACCTCCCG TGGAGTCCTC TGGACCCTGC CTCTTCCCCT CCCTGTGTGC TCCAAGGCCT 960 TCAGGCTTTC CACCTTCCCT GCGGAGATGA GGGTGGTGGC CTCCCTTTTT GTCACCCTTC 1020 CAAGGGTCAT GCTCGTCTGC TGGCTTTTCT CCAAGATGCT GCCAAAAATG ATCTTAATAA 1080 GACACAAGCC TGGTTGTGAT ATTTTCCTGA TTCAAGTGTC TCTGTGGTTC TTGGTTGCCT 1140 TCAGGAGAGA GTTCAAGCCT CTTATGGTGG TTTGTGAGGC CAGGCCTGAA CTAGCCCCAT 1200 CGTCTGTTCA TTCACCACCC CAGTATCCCT GCTGCAGGTT TTTAAAGATC TCATGTCCCT 1260 GATTGCCTGT CACTGTGTCT GACTCGAGCC CTTGTCTCTT CCATAGACCC TCCCTCCTCC 1320 ACCTATCTTA GTAGTACCTC CTTCTGCAGC TGCTTTACTG AGAGGTCTGC CTTCTAGAGC 1380 AGGGGTCACC TGATGCTCTG TCTCCCCAAC AAGGGCTATG AGCAGTAGCT CTTCTCTGTA 1440 GGTCCCTGTG CCTCATTGGA CTCACACAGA 1470
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