Tag | Content |
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EnhancerAtlas ID | HS191-19664 | Organism | Homo sapiens | Tissue/cell | Trophoblast | Coordinate | chr2:15903140-15904670 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr2:15904528-15904542 | CTGAGTCACTTCTT | - | 6.17 | KLF5 | MA0599.1 | chr2:15903819-15903829 | GGGGCGGGGC | - | 6.02 | SP4 | MA0685.1 | chr2:15903815-15903832 | CATAGGGGCGGGGCCAC | - | 6.02 | TFAP2A | MA0003.3 | chr2:15904125-15904136 | AGCCTCAGGCA | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGACTATTG GGGTCCCAAG GAAGAAGGGG ATGGCCTTTC CATCATGGAG TAAGGGCTAA 60 TTTCAGAGGC CAGCATGTAG GTTCCAAACC CGGCTTTCCC TCATTTGATC CTCAAACACC 120 CCATCGGGGG GCCTGGACAG GACTTATCAG GCTTGTGTTA CAGACGAAGA AACAGAGGTC 180 CAGCGAATGG AAGTGCCTTG CCCATGGTCA TGGAGGTCAT GAGTGCAAAC TGGTCTTGCA 240 CCCAGGGGAA TCTGGATTCT AACTCAAATC TTTCTCTGCT GCATGGAGAC CAGGGCACTG 300 AGGGAAATAG GCTTTTCTCA GAACCAGCTC TGCCTGTTTG ACACTCGATC TGGGCTGGGG 360 AGGAGGGGGC AGGAATGAGC ACTGCATCCC AGGGGAAGGG CTGGTGAACG TTCTGTGCGA 420 TGACTGTGCC TGCACTGAAT CCCCTCTTGT CTGTGCTTCT CCCAGGAGGG GATGTGTGGG 480 AGGGCAGTGG GCTGGTGGCA GAATTCAAGA ATGCCCATTC TTTCAGCAGG GAGGCCAGCT 540 GATCGTGGCT TGTGCGTCGT TGGTCTCTGT GGAGAGTTTG GAGTGCAGCT CTCAGAGGCC 600 ATGGCCGGCA GCATCTTCGG CATTTCGGGG CCTCTGCTGA CTCTTGGTTC AAACCACAAA 660 GCCTCTGCCC GAAAGCATAG GGGCGGGGCC ACAGGCTGGC CTCATTGGTA GCCTGGGTGG 720 TGGTCGGTTT ACCAAGGTTG TCCAAATACA GTGGGAGGGT TCCGAGCGCT GGGAAGAAAG 780 CGTCCTGGTC AAAGGGTGGC TGACCCATGT CCTGGTGAGC CTCCTGCAGC TTGCCTTGTC 840 TGCTCACCTG CCTGAACCAT AAAGAAACTC CCGTGATACT TTGGGCCGTG AGCCTGGAGA 900 AGCGTTCTGG TCTTAGGGGA AGCGCATTGA ACCTGGAGTC ACCAGACACA GGCACAGTCC 960 CAGATCTACT GGAGCACAGA TATGTAGCCT CAGGCAAGTC ACTTAACAAA TCTAAGCCTC 1020 AATTTTCTCT CCCCTCAACT GGGGTAATAA TATTGTGAGA AATAACAGAG CTTGCAGACG 1080 TGAAAGTGCC GCAGTGCATG GTACATCATC GATCCTCAAT AAGTATATGT GGAATGAGTG 1140 AATAGTGGAA TGGATCAACA TAAACTGCCC CAGCGTCCTA GGAAGGAGTG TGTACCTTTG 1200 GCAAGGAGCG GCTGGGTGGA TGGAATCAGA GGCATTATGT TTCGTGTTCT GAGGGCCCTT 1260 AAGTATCTGG TCCAATGTCA TCACTGTAAA GGTGGAGAAA GGAAGAGTTG GAGATGGGAA 1320 GGGACTTCCC CAAGGTCACA TGGTGGCTGA CAGAGCTAGG GACACTTCAT TGAGTCCCAT 1380 CCCCTGCCCT GAGTCACTTC TTAATCTCTC TGCAGCCACT CCAGCTTTCA AACACACAGT 1440 GGAGGCCAGA GATAAAAAGA GAGGCATGGA ATCGTCATTG CCATCATTTC ATGTCATTTC 1500 AAACTGATCA GACTTGGGTT TCAATTCCTA 1530
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