Tag | Content |
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EnhancerAtlas ID | HS196-10914 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr16:30502830-30503890 |
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 | GAGTGTCTAC TATGCTACTT ATCCTTCAGA TCTCAGTTTA GCTATCACTA GTGTAGCACT 60 AAGCATTTTA TATACATGTC TTATTTAACT CTCAAAACAC ACCCCATGAG ATTGGTACTG 120 TTCCTTTTTT TTTTCTTTAG ACATAGGGTC TCACTTTGTC ACCTAGGCTG GAGTGCAGTG 180 GCACCATCTT GGCTCACTGC TGCCTTGACC TCCTGGCTTT GAGCAATCCC CCTTCCTCAG 240 CCTCCCAAAG TGCTGAGGTT ATAGCCGTGA GCCACAATGT CCAGCCTCTT CCCTTTTTGT 300 AGATGAGAAA ACTGAGGCAC AGAGGCATGA AGCAATTTAC TTAACTACTA CACAGCTAGG 360 AAGCAGTAGC ACTAGGATTT AAACCTTGTC TCATGGAGTT CAAGAATTTG GAGTTCTTAA 420 CCCTTGTGCT TCCAGACTCC ATACGACAAT AGGGAAGCGG TTCCGTCTCT TCACTCTTCC 480 TTCCATGTGC TGTAGGGCCT TGGACAGCTC TGTTTTCTTC ACTCACTTTC AACTGCTCTG 540 CACAGAGACC ATCAGATGGG GTCAGTGACT CATCTCAGAG GATTCTTGCT GGTGGCTCTT 600 GGCTCTAGCC CAATCTTGGG TCCAATTTCC TGCAGTGTTT CCTCGAACAT TCAATAGAGG 660 TTGTCCTGGT ATCTTAGAGG AAAGAACCTC ATTACAGGAA GTTGAAGATG AAGACAGCCT 720 GACACTGACA TGATATCTTT TTTTTCTTTT TTTTTTTTTT TGAGACTGAG TCTCTCTGTC 780 GCCCAGGCTG GAGTGAAGTG GCGCGATCTT AGCTCACTGC AACCTCCACC TCCCAGGTTC 840 AACTGATTCT CTTGCCTCAG CCTCCTGAGT AGCCGGGACT ACAGGTGCCC GCCACCACGC 900 CCAGCTAATT TTTTGTATTT TTAGTAGTGA TGGGGTTTCA CCATGTTGAC CAGGCTGGTC 960 TCAAACTCCT GACCTCAGGT GATCCACCCG CCTTGGGCTC CCAGAGTGCT GGGATTACAG 1020 GCGTGTGCCA CCGCTCCCGG CCAACATGGT ATCTTTTTTT 1060
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