Tag | Content |
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EnhancerAtlas ID | HS089-05773 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr17:41647650-41649040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr17:41647948-41647959 | CATGAGTCACC | - | 6.62 | JUND | MA0491.1 | chr17:41647948-41647959 | CATGAGTCACC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 41647897 | 41648146 | chr17 | 41647718 | 41647841 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I043570 | chr17 | 41648001 | 41648110 |
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Enhancer Sequence | CCCTTGCAAA TATCTTTTTT TTTTTTTTTT TTTTTTTGAG ACAGAGTCTT GCTCTGCCGC 60 CCAGGTTGGA GTACAGTGGC ATGATGTCAG CTCACTGCAG CCTCTGCCTC CCCAATTCAA 120 GTGATTCTTG TGCCTCAACC ACCCAAATAG CTGGAATTAT AGTTGTGTGC CACCACGCCT 180 GGCTAATTTT TGTATTTTTA GTAGAGATGG GGTTTTGCCA TGTTGGCCAG GCTGGTGTCA 240 AACTCCTGGC CTCAAGTGAT CCACCTGCCT CAGCCTCCCT AAGTGCTGGC ATTACAGGCA 300 TGAGTCACCA CGCCCAGCCA TCCCTTGCAA ATATCTTGAC TGTGATGCTC ACCACACTGA 360 GCTATAATTC TTTGCCCATG TGTTTTTCTC CCACATTCAG CCATCAGTTT CTCTTGGGTA 420 CAGGTTGTGT CTTATTCATC TCTGAATCAT CAGATCCTAG TGCAGTCCTT GCCTCGCAGG 480 AGATACTGGC CTAGAAGCTT GCTGAATGAA TGAATGAATG AATGAGCACA CAATCAGGAG 540 AATGGACAGG ATGAACTGCA CAGACACCCA CATAGTTCCT CACCATCCCA CCTCCTATGC 600 CAGAGTCATT ACACAAATAT TCACTCCTGC AAACGCATAC TTCTCACCCA TAACTCATGG 660 TGGCTGAACT GAATTCTAAC AATTGATTCT TGTTCTGCAC ACATTGGCAT TTTGCTTTCA 720 GAAGAGCTCT GGTAGCTGTA GCAGTCCTTT AATTCATTTA TTTATTTATT TTTATTATTT 780 TATATATATT TTTTGAGACA GAGTTTTGCT CTTGTCACCC AGGCTGGAAT GCAATGGTGC 840 AATCTTGGCT CACAGCAACC TCTGCCTTCC GGGTTCAAGT GATTCTCCCA CCTCAGCCTC 900 CTGAGTAGCT GAGATTACAG GTGCCCACCA CCATGCCCGA CTAACTTTTG TATTTTTTTT 960 TTCTTTTGAG ACAGAGTCTC GCTCTGTCAC CCAGGCTGGA GTGCAGTGGC GCGATCTCGG 1020 CTCACTGCAA CCTCCACCTC CCGGGTTCAC GCCATTCTCC TGCCTCAGCC TCCTGAGTAG 1080 CTGGGACTAC AGGCGCCCGC CACCACGCCC AGCTATTTTT TTTTTTTTTT GTATTTTTAG 1140 CAGAGACAGG GTTTCACCAT GTTAGCCAGG ATGGTCTCGA TCTCCTGACC TCGTGATCTG 1200 CCCACCTCAG CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCACCATGC CGGGCCTAAT 1260 TTTTGTATTT TTAGTAGAGA CAGGGTTTTG CCATGTTAGC CAGGCTGGTC TCGAATTCCT 1320 GACCTCAGGT GATCTGCCCG CCTTGGCCTC CCGAAGTGCT GGGAATACAG GCATGAGCCA 1380 CTACAACCAG 1390
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