Tag | Content |
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EnhancerAtlas ID | HS184-08793 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:124715770-124717490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF410 | MA0752.1 | chr12:124716090-124716107 | GAGTATTTTGGGATGTG | - | 6.79 |
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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 |
GH12I124231 | chr12 | 124715724 | 124719727 |
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Enhancer Sequence | CTCTTCACCT AGCTTAAGAA TGTAGAGATG TCGTGTATGG TTGGGCAGGT TGTTCACTGT 60 CCAAGGGTGT TCCAGCTGAG GAGAGCGATG GGAGCTGAAA GCATCCATGC TCTACTCCCT 120 AAGCTCTGCA CTCTAACATG TGCTCTGGGT CCACCAGAGT AAGGGATGCC CTCTTTTCAC 180 TTGTGCAAAT GCACTGGGTG AGCTAGCAAC AGACCTGGTC GACTGCTGTC TCGGGATATT 240 TTTGTGTTTA CTTGTGAAAC ACCCAGGCTT GGGCTGGATT CCCCCAGAGG CAGATTGTGA 300 GCTGAGGATT TGAGTGCGAG GAGTATTTTG GGATGTGATT CCAGGAACCT CCCAGAGAGA 360 AGCAGCGGGG AGTCAGGCAG GAAAGAAAGC ATGCGTCAGG GAGCTGGTTA CTACTGGGCC 420 ACCGAGGCTC CATCCCAGTA AGGAACCCTG GAAGACGGGA GGAACGCACC TTGGAGTTGC 480 TTCCCTAAGG GATCAACTTC AGTTGGTCGC CACTCAAGGC TCCTCCTGAG GGGAGCAGGC 540 ACAGAGTCCC TGGCACTTCT GGCCCTGAGT GCCCAGGGGA TGAGTGCGTG ACATTGACGG 600 CTTCTGCTGT CCTCTGTCTC CTGCTTTCCC CGTGGGATGA ACTAGCTTGA GAGGCACAAG 660 ATTCCTGAGC AGGCAGAGGG ACTCTGTAGG AGTCTCAGAG CTCCTGAGGC TGCACCCTCG 720 CCCTGGAGCC CCATGAAATC TTCAATTTTG GGTTTTATGA GCTTCACAAA CCTTCCAGGG 780 GCCTCTCCGG CTCCGGATGG GGTGCGTTGG AGGCCTGGTG CCCACGTGTC TCCTGGGCCC 840 TCCACCTGTG CCCCGCCTGT TTGCACAGTG TGCGTGAGCT GAGCACCTGA GTTTGCTCTT 900 TGAATCAAGT GTTTAACTCA CTCACGGTAA TAGTGGCTGA TAATTCTTGA GCTAACACAC 960 CTTCTACTTT GCGGCCTAGC CTTGTTTGCC TTTCAGCCCT GGTTTATTAT CTTCCATCGG 1020 ATGAAGCTTA GGAGCACCAG CGCTGCCTAG GGAAACCCTG GCCCCTCCTT CCCTGGGATC 1080 ATCTGGGTCC CCCAGGGCTC AGGCTTTACA ACCCCTGCTG CTTGGTTACC CACCTCCCAC 1140 CTGGGGCCCC TGACAGATCA GGGGACAAGC AGATAGAGGG CTCACCAGTG CAGTCCAGTG 1200 TATGCTGCCG GGCGGGCCGG AGCAGAGTGA GTCAGATTTG GCTTTTTATA ATCATCCAGG 1260 TGCCAGGGTG GGCACGCGTC CTGGGTCATC CTTCCAGCGA GGGCTCACAT CATAGCCTGT 1320 CACCAGCAGT AATTCAGCAG GAGGGTTTAG TTTCCTCCCT ATGGGATCAG CGAGGGCAGC 1380 TGTCTAAGCC CCAGGCACAC TGCCTAGGGC GGACGTGGGG GTGGGGGCCG TCCTCCTAGG 1440 GCTGCCCTGC CTCTTGGCAG GTGATCAGCC TTCACCTCCT TGTGTGGTTT AGGGGGGCTG 1500 CCTCCTGTCT ATGTCAGAGG GCTTCTCAGA AACAGGCACC GCTGTAGGGG CAGCAAGATG 1560 ACTTCACTTG GAAAATGGAA TGTACTTAAA CGAGATCAAG CCACCTCGTG GAGAAGCCAT 1620 TCCCTTCCAA TTTGTTTTAA TCCTGCTGAT TATTGCAAAG AGAAAGACTT AGCCTGGTGC 1680 TAATGAGTCT TTAATGCCTC TGAGGACTTC CTAAGTTTTC 1720
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