Tag | Content |
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EnhancerAtlas ID | HS191-10485 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr13:35321210-35322650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr13:35321452-35321467 | TCTGCTGAGTCATGC | - | 7.23 | NR2F1 | MA0017.2 | chr13:35321586-35321599 | CAGAGGTCAAGAG | + | 7.04 | Nfe2l2 | MA0150.2 | chr13:35321454-35321469 | TGCTGAGTCATGCAG | - | 7.41 | TFAP2A | MA0003.3 | chr13:35321612-35321623 | TGCCTGAGGCT | - | 6.32 |
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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 |
GH13I034747 | chr13 | 35321416 | 35323510 |
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Enhancer Sequence | TAAAGCATCA ACTATAGTAA TGTGGAGTGG GACCTGCGGT GGGCAGGGCC CTAGAACTCC 60 CAAGATTATA CGCCCTTTGT CTTCCACTAC CAGGGTGGGT AGGGAAGGAC CATCACGTGG 120 GGGAGGCGTT AGGCATGTCT GAGCTCACTC TCCTTGGATG AGACTTGCTG CAGCCGCTGT 180 GGGGGATGAA GGAGAGATTC CCAGGTCACT AGAGTTGTGT ACTTCAGAGG ATTATGGCTG 240 CCTCTGCTGA GTCATGCAGG TTGTCAGGGA AGTGGGGGAA AGCCAGCAGT CACAGGCCTC 300 ACCCAGCTCC CATGCAAGCT AAAGGTCTGG TCTCACTCCC ACTGTGCCCC CTCAACACCC 360 CTAGTCTGTT TCCAGACAGA GGTCAAGAGG GTCTTGAAAA CTTGCCTGAG GCTGTCTGGA 420 CCCCAGCTGT GAAAGAAAAG GGCTTTGGTT TATCCCCCCG CCTGTGAAGT CTGCAAGCAG 480 GATTCATGCC CTCCCCTGAG TTCTGGCCAG GAAGATTCTT GCCCTGTTCA AATTGTTACA 540 AATTCAGCTA CAGAATTCCT TATCCCTTTG GAGTTTTGCC CCAAGCTCCT CTGGCCACCA 600 TCCTGATAGA TCCCTGTGGT GCCGGGCAGG AATGGGCTGC CTGGGGACCC AGTGAGCTCC 660 CAGGGCCTTT CTGCTGCTTC CTCTACTGCT GTATTTCATT TGGCTTGGCT CGCTACCTTG 720 ACTGAGCTCA AGGTAAAGTC AGAAACCTCT CCCACAAACA GATCTTCATC TTCTCCAGTG 780 GGGGTGTGTG TCCAGGAGAA GCGGGTCTCC CTTTCCCACT TCCACAGTTG GGGCACTCAC 840 AGTATTTGGG GTGTCTCCCA GGCCCTACAG GAGCAGTCTG CTTCCTTCAG AGGTTCTGTG 900 GGTCCTCTCA GGATTCCTGG TTTGTTCTTG CAGTTGATCT GGAGCTAAAA TTCACAATGC 960 AAGCCTTCGC ATGCTGCTCT ATCCAGAGCT GCAATCTAGT CCTGCCTCCC ATCCTCCATG 1020 ATCCCCTAAT CTTTGCATCG TCTTTTTTTT TTTTAGACAT AGCACAGAAA AATGCTTGTT 1080 TACTTGGCAG GCACCCTGGT AGCCAGATAG AAGTGCTTGG GCTGAGCCAA GTGCCTTGGT 1140 TACAAGTACG TCATCAGCCA CAATTAAACC AGGAAATACA GGGCTCTCAG GAAGTACACT 1200 CGATAACGAA GCCTCAGTGA GCCAAAATTA GCCAATAATC AGCGCTACTC TTCATCCTGA 1260 AATGATGCAA CCATATTTTA CAAGGCAGTC CAGTAGTGGA AGACAGGCCT GAGGGACACA 1320 CTAGACCCCT TGTCTAGCTT TGTCACCAGC TCACATGATT TTAGACAACC AGGGTTAAAT 1380 GCCTTCCCAG TGTTTCAGCT TCTCTTTTGC AAAGTCTCAA ATCTAGCCAT CAGTGGCAGG 1440
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