Tag | Content |
---|
EnhancerAtlas ID | HS139-25609 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr18:77367150-77369480 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LHX2 | MA0700.1 | chr18:77368107-77368117 | ACTAATTAAC | + | 6.02 | mix-a | MA0621.1 | chr18:77368107-77368118 | ACTAATTAACT | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCAGCTAACT CTTGTGCACA CACTAATGCA CACCAGCAAC ACGCCAGGGG CCTCAAGGGC 60 CAGGGCACAG GGAGGGACCT CTGCTCCTGG GACAGCAGCC CTGTGGGGGG ATCCAAGGCC 120 TGAGCCCCGG TGAGCAGCTC CATCAGGGCC CGAAGGCCCC GTCTCCATGG GGCCAGAGGG 180 ACGGAGGCTG ATCACTCGAG CCAGGCACTT CCCACAATCT TCCTGTCCCT GCCCTCAGTA 240 CCCCTGAGGA GCGTGGCCCC CTCCTCACTG TGGGTCCAGG CCCAGAGAGG AGGGCGCTGG 300 GGCTGCTGGG CCTTTTGGGG CAGGCCACGG GCACCCTCAG CTCCGCAGAG ACTCCTGAGA 360 GCCAGGGAGA TGCCTTAGAA AGGAAGCTCC AAGTCTTCTT GCTGGAAGCT TTCAGCACCG 420 AGTGCAGATG CCAGCCCCAG TCCTTGGCCC ACGGACCAGG GCACAGGAGT CTGAAGCCAC 480 TCACAACATC CCCTCCTCCA GGGCTTAAAA CGCAGCCGGG GCTCACGCCC TCTTGGGGGC 540 TTCCGCGTGG CCTGTACCTG TGAGGATGCC GGCAGGCTTG GCGCACGGGT GGCTCCGGGG 600 TCAACTCCAC GGGCGCTGCC CCCACCCTCG CTCCCGCAGT GCCTGAGCCC CACTGCCCTC 660 CCCACTGCTG GTGTGCGTGC ACCTCAGGCC CCTCCGGGAG CTGCACAGAG TTCACGCCGG 720 GTCAATCCAC CATCCACTGC ATGGAGAGGC CAGCGGCCTG GGGCAGCTGT GCTGGGTAAG 780 GCAGCGAAAC CCTTAATCTA ATGATGTTTT TCTCCAACTG CAACCCTTGC ACGCTAGGAG 840 CCACTCTCTC TTAATTAAGC TCAGCTCCCA CATGCTTTTA ACCATGCAAC TTTAAAAGAA 900 ACATGTATCT TTCCAAATTA ACTTTGTGTC TAAGAATAAT AAGAGAGCAA GAGTTGTACT 960 AATTAACTTA CAGTCGGCTA CAGAACTCAT TTGCCAGTGC CGTGTAGGCT TCAAGGGGAG 1020 CCGACATTTA TTCAGTACAG AGGACATTCC AGGGCACTGG TCCCACCTGG GCATCACCCC 1080 TTGTTTCCAC AGAGCCCCGA GGGTCTCAGA GGCAGGAGCC CGGGGACAGT GCGGAGCTGG 1140 GACTAGGATC AAGTGTGTCT CCCTTCCGAG CCCATTCCAT ATTCCAGAAG GATCCAGAGC 1200 CTTCCCTCCC ACATGCCAGC TCACGGCATT GGCTACAGTA ATAGTCAGTC TGCCTAGAGT 1260 GTGTGCTTTT GATTGAAAAA GCCAGGAGAA AATCTTTTTC AAAGAGTGGA ATGTTCGAAG 1320 AATGGAAATC TGTGAAAATC AGTCGTGTGA TTTCTCAGGG CTCATTTCCA TGAGCCGCAG 1380 TTACATTCTC GACTGTGGCC AAGGACGCTG CCTGCCCAGC CTTCGCAGGG TGAGGCACAG 1440 GTACACGCGG TTTCCGGGAC CTGGCCACGG GCCACTCTCC AGGACTGACT GCAAGGACCT 1500 TCACCTCCGA GGAGCCGGGA GAGACGGAGA CACCCAATCT GAGATGTTCT GACAGCTGCT 1560 TCACAGGCTG AGCTGCGGGA GGATGGCAGC GCCCTTCCTC CACGCTGAGC TCCGGAGCTT 1620 GGAAGCTGAG GCCACCAGCT CCGTCCCGGC CAAGCTCTGA GCATCACAAG CTCAGAAGGA 1680 ACAAACTGCA GAGTCCATGC TGGACACAGA GCGCAGGGAG AGACCCCTTG TCCCTCACCC 1740 ATGGCACGGA GCATGTGATG GCAGATGCCT CTGCTCCAAG ACAAAATGGG CAATGCCTTT 1800 GCAACTGACC AAGCAAACGC AGACACCAGA ACTGCTTTCT AAAATTCCAG GGCTGTAAAT 1860 CTCACATGCC CCAAGCAGGC AGAAAAACAG AAGAACGCTC TTACGGAGCG AGTGTACCCA 1920 GGGGTTTCCT GGACTTGGAG GGGGCTGAGC CTGGGAGGAG GAGGGGCTGC GTGTGTGGGC 1980 AAAGTTGGCG GAGCTGGTTG CTGCATGGCT GAGGGAAGGG GCTGAGAGGC CGTCAAGGCT 2040 CACCTGGACG TTCAGTGGCT TCCCAGTGCT TCCCCTCCAG CCTGCAGCCG CCTGCACCAA 2100 CAGCTGGGCC CAGGTGGGAT TTTCCAGCAC GGGAGGGGCG AGGCAGCTTC CCCAGGCCGA 2160 GAGGCTGAGG AGAGCAGCAC CCAGCAGCAG GTGGACCTGA GGTGGGAACA CAGCTCAAAG 2220 GAAATGGCAG CAGCCAGTGT CTGTGAGGGG ACTGGCCATG TGGGCCCAGC TTTGGGGCTC 2280 AGGGAGGCCC CAAGACTCCC CACAGAGTGA AGCTGGGCCA GGTCAGATGC 2330
|
| |
|
|
|