Tag | Content |
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EnhancerAtlas ID | HS134-01037 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:40387580-40388810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr1:40388613-40388625 | TGCCGTGATTTC | - | 6.32 | SP2 | MA0516.2 | chr1:40387938-40387955 | GGAGGGGCGGGACTAGG | - | 6.07 | ZNF263 | MA0528.1 | chr1:40388127-40388148 | GGAGGAGGCAGAGGTGGGGGT | + | 6.77 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 40387800 | 40387974 | chr1 | 40387646 | 40387810 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I039923 | chr1 | 40387912 | 40388030 | GH01I039922 | chr1 | 40388161 | 40388350 |
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Enhancer Sequence | CTCAAGTCCC TGGGCCTAAG TATTGGAGCC GCCACACAGA AAACCCAGGA ACAAGCAAGA 60 CACTGGAGTT AGGCACATCT AGGCTGCGCC ACCCCTAACT GTGTGACCTG AGAAAGGCAC 120 CTAAACCAAA CTGGTCTTGT CTCCTAACCT GTCAAATAGG GAGATTCCTG CTTATCATGC 180 CTGACCGTGG TGAAGATTAA ATAGGATCAT CCATGCAAAA CTCTCAGCTG GGCGTTTCCA 240 TCACCTAGAA GGTGTTCCAT GATGTCAAAG CTATTATTGT TTTCATACTT GGGATGGGGA 300 GTGCCGAATT CAAATCGGTT CTGAGTGCGG GTCTACTCTG ACACCCTGTG TGTCAGAAGG 360 AGGGGCGGGA CTAGGAGGCA ACAAATCCAT TACAGCACAG TTGGCAGATG TGTCCAGTCA 420 CACAGCCGGG AAGTGGACCA GGGACTGGAC AGCAGCCCTC CGCCCAGGAC TCGGCCAGAT 480 GTTCCAAGCC TAGCAAGGGG CGCTTCTACC CCCACCCATC CTCCCCGACA ACCTAGGCCT 540 GTGGCTTGGA GGAGGCAGAG GTGGGGGTCG GCAGCCGGAC GTCGCAGGCC CCAGGCTGCG 600 CGCAGGAAGC GGCTCCAAGG TTGTCCTAGA GCCTCAAAGC GGCGGAAGGG AGGGAGCAGC 660 CGGCACCTGC ATTGTGCGAG CCCCGCTCCC CGCTGAGCTT CTGTGACCTC TGGCTCGCGC 720 TCTTGGCATC CGCTGCTGGG GCAGGGCCCG CGGCTTTCAG ACAGGTATTA ACCGGGCAGA 780 GGATACTAGA TCTGCGCTGG CTTTCATTCA TTCACGCATC CACTCATTCG TGCATCCATC 840 AGTTATCGAG CTGCGGCAGG AGTTAGTGCA CAAAAACATA GTCCATGATC GCAGGGACCA 900 TACTCCTGCT AAATCATGGA GGTTTGGGGA GTTCCTTCAG ACTCTCAGTA AACTTATTCG 960 TGGAGGTCTG ATTTTTTTTT TTTTTTTTTT TTTTGAGACT GAGTCTTACT CTGTCGCCCA 1020 GGCTGGAGTG CAGTGCCGTG ATTTCATTTC ACTGCAACCT CTACCGCCCA GGTTCAAGCG 1080 ATTCTTGTGC CTCAGCCTTC GGAGTAGCCT AGCTAATTTT TGTATTTTTA GTAGAGATGG 1140 GGTTTCGCTA TGTTGGCCAG GCTGGTCTCA AACTCCTGAC CTCAGATGAT CCGCTCGCCT 1200 CAGCCTCCCA AAGTGCTGGA GTTGGTTACA 1230
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