Tag | Content |
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EnhancerAtlas ID | HS019-08554 | Organism | Homo sapiens | Tissue/cell | CD20+ | Coordinate | chr19:45001430-45002910 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr19:45002461-45002474 | TGCAGCTGTTTCC | + | 6.19 | Myod1 | MA0499.1 | chr19:45002747-45002760 | TGCAGCTGCTCCC | + | 6 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGAGAGAAGC CCCAAGTACA GCATGAAGAT GTAGGTCTGC CGGAACCGCT GGGCCCCCCA 60 CCCCCATTAG CCCCTGCTCC CAGGATGCAG GATGCATTCC CATAGCAAAT GCACTTCTGG 120 AGGTTCCTGC CAGCTTCCTG CCCAAATACC TGTGTATGTA CTGAGAGTCC CTCAGTCCCT 180 CTCCCAGGCC AAGTTTCTGC AGCTCCAACC TGGTTCCTCC ACCATCTTGG GCCCCTGGAC 240 CATCTACCTG TAAGCCCAGC TTGTGCCCAA CATGGCCTTC TGCCCACCAC CAAAGTCTGC 300 AGCACCAGTC CATCCCTCTC CTATTCACTG GGCCCTGGGA TCCCCACAAA TATCAGGCAT 360 ATCGAGGACC CCCTGGTGTT CACCCCATCC TACCCCTACC AACCTCAATC TACAGCCCCA 420 AACCAGCACT TCTTCCTAGG GCCAGAATCA CACTCACTGC CTAACTGCAT GAAGCTGGTG 480 ACACAGCTCC ACTGCTCCCA GGAACTGATT CAACAACTAA GACTGATCCT ACCGTTCCAT 540 CAGCCAGACC TGTCCCTCCA GCAACTCAGC ACAGAGGGCC ACCCACATCC TGCTCAAATA 600 GCCAAGCATT TATGCACAGA GCTCAGCTAT ACCCACATCC TGTTCCCTCC ACACTTCTGG 660 GGTCCACTGG CTCCTACTCG AACAGCACCA GCCAGATTCC CACCCTAACA CCCTCCCAGG 720 CCCTGAATTT GTAGCTCTAA ACCAGTCCCT CCACCAACTT GGGTATACTC AGGCCTGAAA 780 CTACAACAAG GCCTGCATAG GGCTGGGGGC CTCCAACAGA CACCAGCACA AGCCAGACAA 840 AAGCAGCCCT ACCCAGGCTC TAAATACATG TCTCAGAAGC TCAGATGCCT CTGTACCAAC 900 TAGGTGTTTT GGGATCCAAG ACTAGAGGGC AAATCCTACC CTAGGCACCC CAACCTCTGC 960 ACTCCATCTC TCCCACTTAC TCTCTCCCCT GCTCCCACCA TATTCTCACG CAGCATAGCG 1020 TAGGTTCACA ATGCAGCTGT TTCCTGAAAT TGCACCCAAA CTGTTTCCTC CACCTTACTC 1080 CACAGCCCCC TGCTTGAGCC ACACCTGCCC AGATTCTGAC CAAACATCTT TCGGGGGCAC 1140 CTGTGGCTCA GGAAGATCCT GTCTTTCCAC CAAACTGGGC ACCATCAGGC TGTGATCAGG 1200 GTTCCAATCA CACAAAGACC CCAGCACCCT CTGTCTAAAA CTCATCTCCG GCCTCCTGTT 1260 TCCCAACCAA ACACCGGTGT GTGTGCACAA GGGGTGCCTG ACACAGTCCC GCCCCTCTGC 1320 AGCTGCTCCC CCCCACACAC CTGGGCATCC TCAGGCAGAA TCAGGGTCCT AGGACTGCCC 1380 ATGCCTCCCC AATCTGCCCA AATGCCAGCA CACGTGCAGA GTGTTGCTGG AGCAGCCCCG 1440 TGCCTCCTAA GACCAGATCC AAACTGGAGC CCCCAGGCCT 1480
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