Tag | Content |
---|
EnhancerAtlas ID | HS139-09968 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr11:70448950-70451470 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr11:70450269-70450290 | CTCCCTTCTCCTCCCTCCTTT | - | 6.92 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH11I070603 | chr11 | 70450021 | 70450150 |
| Enhancer Sequence | GAAATGCACG TGGACCCACA GGCTTTGGAT AGCGACTAAG AAGCTGTCTA TCATATGATA 60 GAGTCCTACA CAGGTGGGAA AATGAATAAA CGAGACACAC ACACCGGGGA GGCAGAACCC 120 CAGAGCATAC TGCTGGCCCG TGGCAGAGGT CGGCAAAGAA TGCAGGTGGC AAATGTCCAT 180 TTACAGAAAG CTGGAAAACA GGTAAACGTT AGCTTTGTTT AGTGATATCA ACACAGGTGG 240 TAAAACCCCA AGGAAAATCC TGAGGAAGCG GTGGTGGGGG ACCCCTCACA GCCCTACTGG 300 CTCTGCACGG TGTCCCTTGG CTCAGGCCAG CACCTCCGTG ATGCTTCCAT GACATGGGGA 360 GAAACCGCCA ACCATGGGCC ATGTACACCA GATGGGTCCA GGCCCAGATG GCAGTTGAGC 420 CCGAGGCTCA GGCCCCATGA GCAGTTGTGG GCAGGAAGCT TGGCTGCCGT CCTGAGACCA 480 ACACCAAGCC ACAGCCATCA CCGCTCCTCC TCCAGGCTTC CCTTCCTCCT CTGGGGCAGC 540 AGCCCATCTT CCCAGCTGCC CGAAGGAGAA AGGCATATCC CCAGTGTCCC TCCACATCCT 600 GACCCTGACC CTGTCCAGCA GCTGGTCCAC AGCTGCAGTA AACCCAGAGT CCAGCAGAAC 660 CTTTGCTCAG TAGGCACACA AATCATTCTT GAGCAGGTGA GCCACTAATA ATGTGTCACT 720 GACACCAAGG AACAGAGGGT TGAGTGACTT GCTTCAGGCC ACACAGCTAG TGAGGTACTG 780 AGCTGGGACC TCGGAGAAGG TGCCTCCTCC ATGCTAGGCA GCCCTCTCCT GGGCCAGTCC 840 TGCTCCCCAC TCCCAACAGC CTTGGTGCTT TCAGAAAAAC TCAAGAGGCG CCAGGAGAAT 900 CCCACAGTCC CCCTTCTCAG CCTAATTTGC AGGCAAGGAA ATGTCTGTGG AGCTCTCCAC 960 TCATCAGGAT CCATCCCCTG CCCAGGGGAC AGGCAGAGAC CTGCCCGATG CCCTGGTGGT 1020 GGCCGCAGGA ATGCTGAGCA GATGGTGCTT GGCACCCAGA AGTGGGGTGA GGAGAGCAGA 1080 ACGACCCGAT AAAATTATTT ATGCAAATAT TTAACCACAG GCACTGCAGC AATGCAAAAG 1140 TAACATCGAG GGGCCCATGA AATGTTAGCT GCCTGCCGCC CCAAGTGCCT GTGTGCAGAG 1200 CCAGCAGCAA GCCAGAGAGG GCGGGAGGGT TTGGGGAGGA GACGGTGCCT TGGAGGGAGC 1260 AGCCTGGAGG GAGGGACAGC CCCTCTGTCT CTGCGCAGGC CCAGCTGCTC AGGCAGAGTC 1320 TCCCTTCTCC TCCCTCCTTT AATAAACACC CATGAAGGGC TCTCTCACCC ATGGTGGGGC 1380 ATTTCCATGG TGAGCAAAAC TGGGAGACAC AAGTGAGCGG TGCAAGAGCA CGAGAGTGAA 1440 GCTGGATGCC CGTGGGGGGC TACCCTGCGC TCCCTGCTCC TCCCAGCCTC TCTGGCAGAT 1500 CTGCACATGG CAGATGGGAA CTGTGGGGCA CACAGCTACG TGGAGGACCC TCCAGAACCC 1560 TCTGCCCTCT GAATGGTTGG GACAGTGAGT CCAGGAGGGC CAGGGGGTGG CCTGGGAGAG 1620 GTGGTGCTGG TGCTCTGGGC TGCAGTGGGC ACTATGATCA CGCCAGTTTA CAGACATAAA 1680 CGCTCGGCTT GGGGAGGGCA GGCGCCTGAC CCGAGACCTC CTGGTGAGTG GTTGCTGTGT 1740 AGAGACAATG AGGACCGCAC TGAAAGCAGT GGCAACAAAG CTTCCCCAAT GTCATACATG 1800 ATGCGTTGAT ATACTACACA TGTATACATA CAACATGCAT TCTACATACA GCATAGCGGC 1860 ATGCCGCAAG CATACGCAGT GCTTTTCATA AACAAAACCA CTGAAGTCTC ACAATGGCCC 1920 CTGAAGGGGG TCAGTCATAT GATCCTCACC CCATTTCACA GATGACAAAC TGAGGCACAG 1980 AAGGGCTGAG GGTGGCAATG GGACGGAAGC CCCAGTGGCC TGGCTCTGGC CCCCTCCCAA 2040 TCCATCTGCA CTGGCCACAC AAGGGTGCTG GACACAGGGC AGTGGTGTGT GGGCAGCGTG 2100 TGAGTCACAA GGCAGGTTCC GCGGTTTCAG GGCCCATCGG GATTCACCAG CAGCAGCACC 2160 AGGCTCTACA GTCAGGACCA GATGGGCCTT GGTCAGGCAG CCTGGGGCAG GGCCAGGGGC 2220 CTGCAGCAGC CCTCCGAGGA TGGGAGGCTC TGAGAATCCT CAGTGAAGGG CAGGGCTTGA 2280 GCCTGGGATG GCGCTTTTTA ACAGGGCCAC GTGTCTTTCT ACATAAAAAA AGCCCCCTGT 2340 CATGCCAAAT CTTAAAGTAA ACATGCCTCT TCTGGAAGAT GCTCTCCCTG CTAGGCCTGG 2400 CCACTCCATC GTTGTGAGCC CCGGGGGTGG GAACACCCAG AGTGAGAAGT GAAGCCTCCT 2460 GCAGCCCAGC CCGGAGACAG CCTGGCTGGC CACGCCCAGA AGGCAGCAAG CGGGTGAGCC 2520
|
| |
|
|
|