| Tag | Content |
|---|
EnhancerAtlas ID | HS098-21696 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr16:47071240-47072460 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr16:47072070-47072088 | GGAAGCAAGGGAGGGAGG | + | 6.73 |
| | | 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 |
| GH16I047037 | chr16 | 47071242 | 47072511 |
| Enhancer Sequence | TGGGACCACA GGCGTGCACC ACCGCGCCCG GCCGGGACAT ACTTACACTA AAAAAAGTAC 60
TTGCTGTCTA TCTGAAATTC AGATTTGGGT GGGTCGCCCT GTATTTCTCG AGGCAACCCC 120
TCAGCAGCCC TCAGGGGGGA CTCCCTCCGC ACTCCAGGCC CTCGGGTGGC GCCTTCGCTG 180
GTTTATCTGC GGTTCACTTG CACCTTCTTC AGAAGTGGCC GACAGCCCAC AGCGAAGGCG 240
GCCCCGTGCC AGACTCTTCT CTGGGGATGA GGCTCCGGGG AGGAGACTCC GGGGATGCGC 300
CTCTGGCGGG ATCTCCCCTG GAAGAATCTG AGTCCAGTGG GGAGAGGAAC ACGTCCCGCA 360
GCTGCCCCGT TCCACGGTGG GAGGCGTCAC GCGGCCGGGA ACACAGGGAG GCGGGGGGCT 420
CCGGAGGCGG CGGCTGGGAG GACCCCGCGG GAGGGCGCCG GGGAGGCCGC GAGGACCGCG 480
CCGGGGGGCT GCGCCCAGGC AAGCTGTGTC CCTCCGAGGC GAAGATAGGA AGCTGCCCCG 540
CGGCGCGCGG TCCCCAGGCA GGGTGCTCGC GGGCGGAGTC AACACAGCCT GGCTTCTGCA 600
CCGGCTCAGG CCGCCAGAGG GCGCGCGGGT TCGGGAAATG GCTTCCCCCC CCGCAGGAGG 660
AGGGCCGAGC TCCCCGCGGG GCGGGAGGAG GAGGGAAAAC CGAGGACAAG CCCCCGCCTT 720
GGCGTCGAGG GTCTCCACCA AAGCCCCACG CGAGAACGGG CCGCGTGTTT CTGGTGAGAG 780
GGGTCTCGAT AGTGCCATCC ACCGCGAGGC CCGACTCCCA GCGGCGTCCA GGAAGCAAGG 840
GAGGGAGGGC GGGAGCGGGG ACGCGGCCGT TCCCACCCGG CTCCTCTCAC GAGACCCGTG 900
ACAAATCGCT GGTCGGAGAG AGAGTGCACG GCCCCAAGGA AGGGAGGCAC TCAGAGCCCT 960
GTCCTTCCAG ACATTCAGAC TATTAACTGA TGGTTGGTCT AGAGGGGACA GGACGGCAGA 1020
GAGACAGAGA AAGCTGGCGA AGGACGCGCA GGATTTCAGA TGTAATGCGT GACTCAGAGA 1080
GATTGCATAA CTTCTTCCAG GCCTCAGTTT CGACGTCTGT CAAATGGGAG TACATTTTCC 1140
CTCAGCGGGA GGATCGTTTT GAGTCCAGGA GTTTGAGGCT GCTGTGAGCC CAGATCGTGC 1200
TACTGCACGA CAGCTTGAGG 1220
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