Tag | Content |
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EnhancerAtlas ID | HS091-17027 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:30502430-30503750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr16:30503393-30503404 | AGTGACTCATC | + | 6.02 | JUND | MA0491.1 | chr16:30503393-30503404 | AGTGACTCATC | + | 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 |
GH16I030491 | chr16 | 30502930 | 30503688 |
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Enhancer Sequence | TTTAATCTCT AGCTGGGTGT GGTGGCTCAC ACTGTAATCC CAGCACTTTG GGAAGCTGAG 60 GCTGGCAGAT CATTTGAGGT CAGGAGTTCG AGACCAGCTT GGCCAACATG GTGAAAGTCC 120 GTCTCTATAA AAATGCAAAA AATTAGCCAG GCATGGTGGC ATGCACCTGT AATCCCAGCT 180 ACTCGGGAGG CTGAGGTAGG AGAATCTCTT GAACTCTGGA GGTACAGGTT GCAGTGAGCC 240 GAGATCGTAC CACTGCAGTC CAGCCTGGGT GACAGAGCAA AACTCTGTCT CAAAAAAAAA 300 GAAAAAAGAA AAAAAGTTTA ATCTCTAGTT AGACACCCAC CCCACTATAC ACACACATAA 360 ATATATACAT ATATGTGGAT AGATAAATAA ACAGAATCCT GAGTGTCTAC TATGCTACTT 420 ATCCTTCAGA TCTCAGTTTA GCTATCACTA GTGTAGCACT AAGCATTTTA TATACATGTC 480 TTATTTAACT CTCAAAACAC ACCCCATGAG ATTGGTACTG TTCCTTTTTT TTTTCTTTAG 540 ACATAGGGTC TCACTTTGTC ACCTAGGCTG GAGTGCAGTG GCACCATCTT GGCTCACTGC 600 TGCCTTGACC TCCTGGCTTT GAGCAATCCC CCTTCCTCAG CCTCCCAAAG TGCTGAGGTT 660 ATAGCCGTGA GCCACAATGT CCAGCCTCTT CCCTTTTTGT AGATGAGAAA ACTGAGGCAC 720 AGAGGCATGA AGCAATTTAC TTAACTACTA CACAGCTAGG AAGCAGTAGC ACTAGGATTT 780 AAACCTTGTC TCATGGAGTT CAAGAATTTG GAGTTCTTAA CCCTTGTGCT TCCAGACTCC 840 ATACGACAAT AGGGAAGCGG TTCCGTCTCT TCACTCTTCC TTCCATGTGC TGTAGGGCCT 900 TGGACAGCTC TGTTTTCTTC ACTCACTTTC AACTGCTCTG CACAGAGACC ATCAGATGGG 960 GTCAGTGACT CATCTCAGAG GATTCTTGCT GGTGGCTCTT GGCTCTAGCC CAATCTTGGG 1020 TCCAATTTCC TGCAGTGTTT CCTCGAACAT TCAATAGAGG TTGTCCTGGT ATCTTAGAGG 1080 AAAGAACCTC ATTACAGGAA GTTGAAGATG AAGACAGCCT GACACTGACA TGATATCTTT 1140 TTTTTCTTTT TTTTTTTTTT TGAGACTGAG TCTCTCTGTC GCCCAGGCTG GAGTGAAGTG 1200 GCGCGATCTT AGCTCACTGC AACCTCCACC TCCCAGGTTC AACTGATTCT CTTGCCTCAG 1260 CCTCCTGAGT AGCCGGGACT ACAGGTGCCC GCCACCACGC CCAGCTAATT TTTTGTATTT 1320
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