Tag | Content |
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EnhancerAtlas ID | HS098-47321 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr5:179603890-179605000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr5:179604506-179604517 | CTGCAGCTGTC | - | 6.62 | Tcf12 | MA0521.1 | chr5:179604506-179604517 | CTGCAGCTGTC | - | 6.14 | ZNF263 | MA0528.1 | chr5:179604095-179604116 | GGAGGAGGACCAGGGTGAGAG | + | 6.51 |
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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 |
GH05I180176 | chr5 | 179603796 | 179605111 |
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Enhancer Sequence | ACAGCAGAAG CTATGAAAGC ATGACTGCTG CGTGGTGCCA GCCGTCAGGG TTGGGCAGTG 60 GTCAGTCCTG CCCATGTCTC CCCCTGGCAT AACCCAAGAC AGGGCCCCTG GCCTGGCCTC 120 CAACTCCCAC CCAACCTTGG TCAACCTCCC AGAGGAGAGG GCTGCAGACG AGGGGTTTCC 180 AAGGGACGGC AACTTTTGCC AGCATGGAGG AGGACCAGGG TGAGAGGTGA GACTCTCAGA 240 GCCTGACGGA GGGGCTGGAT GAGGGGCAGT GGGATGGGGG GCTGGCTGGG CTACTTCCAG 300 AAACGTCCAG CCGAGTAGAG GATGCATTCA AACCATGTGC ACATCAGCCC CTCAGCCCCG 360 AAGCCAGGGG CTGCTTTCCC TTTCCGGCCC CACCTCCCCA CCCAGTGAAG GGGCTGGCCT 420 GCCCGGCTCA CCCAGCAGCT TCCCCAAAGA CACAGGCTGT TCATCGGCTC CATTTTTAAC 480 CTTCCTTAGT CCCAGCAGCC CCAGCAAAAG CTCTTCGGTG AGTGCCTGCG CAATCTGCCC 540 GGCTGGGCCG CAGCAGTCCA CGGGCAGGGC AGAGCCCCGG GCTTCCTTCC GGGACCCCTG 600 CCAAGGCTCA GCCCTGCTGC AGCTGTCCAA GGCCATGGCC TCTGCGGCTT CTGCCTGGCC 660 AGCATCTGTT CTTCCCTCTG AAAACAGAGC CCATTTGTCC TTCCTCTCCT GCCCGTGGTA 720 GGAGGACATG GCCCTGGTGC CACTTGGGGA AGGAGTTGCG TTGGTCTGTG ACAGTTGGGA 780 TGGCATGTGA TCCAGGCCCA GCCACTCAGT GCCTTTCATC TCCCTGGCCT CTGGGATAAA 840 TCCATGGGCA GGCATGTCAC CTGGGTGGGC CACCAGACTC AGTTCGTGGG ACATTTATTT 900 GAACTGTCTG AGCAGAGCCT CTCTCTCTGC TCAGGGCAAG GTAAGGACAG GAAGTAAGTA 960 TGGAGCTGGT GGGGGCTTTC TTGTGAAAGG GGCCCACATG GAGGAAACGG AGCCAAGACT 1020 CACAGAGACC GAGACCATGT CCCACATCCA GCCATGCCTG AAGCCCACCT TGGGCTTTTT 1080 TTTTTTTTCT TTTTGAGGTG GAGTCTCGCT 1110
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