Tag | Content |
---|
EnhancerAtlas ID | HS047-05761 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr11:34259810-34261240 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr11:34261039-34261054 | AGCTATTTTTGTATT | - | 6 |
| | 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 |
GH11I034238 | chr11 | 34260119 | 34260865 |
| Enhancer Sequence | CCTTCAGGGC TTTTCCCAAA TCTCTGACCT GTATTTGCCC ACTTCCAGCT CTCCCTAGTC 60 AGATTCTCTG CAATAACTTC TCCATAAAAC TAACCATCAA ATATATGATT CATTCTATTA 120 TTTTATTGCC TGTCTTCCCA AATACTATGT AATCTCCATG AGGGCAGGGC TTTTGTCTGT 180 TTTATTCATT GCTATATTCT TAGTATCTAG CACAGTACCT GGGATACAGT AGGTACTCAA 240 TAAATATTTG TTGAATGGAG ATGTGCCATG ACTTATTCAT GTGCATTTGA ACAAATACCA 300 ATCCGGTACC TACCACGTGC CAAGTACTCA ACATATATGA GCCATTAAGT CTTGCAACAG 360 CCACTTTATA AATGATGAAA CTAAGACATG GAAGCAGAGT GACTGGCCTG AGCTCACAGC 420 CTGAGCTGGG ATTCAAGCCT CGCTCTTTCC CAAGACTATT CTTTCCTTGT GTTTGATCCC 480 ATTAATCATC ATTCTTTTTT TTTCTTTTGA GTCGGAGTCT CACTCTGTCG CCGAGGCTGG 540 AGTGCAATGA TGCAATCTCG GCTCACTGCA ACCTTGGCCT CCCGGGTTCA TGCCATTCTC 600 CTGCTTCCGC CTCCTGAGTA GCTGGGACTA CAGGCGCGTG CCACCACACC TGGCTGAATT 660 TTTGTATTTT TAGTAGAGAC GGGGTTTCAC CATGTTAGCC AGGATGGTCT TGATCTCCTA 720 ACCTAATAAT CTGCCTGCTT CGGCCTCCCA GAGTGCTGGG ATTACAGGCA TGAGCCACCA 780 CGCCCAGCCC ACATTCTTTT TGTAATCTCT GACATCTGTT TTCCCTGCTG GATTAGAAGC 840 TCCATGAAAG CCAGGACTGT CTGGGACCCA GGAGGTACCC AGTAAGTATC TGTGGGACGA 900 CAACACCTGA TAAGGACCAG GGGTGGGAGG TGAAGTGGGC TCTGAGTGGA TGATTCACTG 960 TCTTGGCCTT TACGTAGCGC CTGGGTTTGT GCGCCCACCT CTGAGCTTGT CAGGGATGGA 1020 TAATGCAGTC TACCCTGAGG CTGAGCCAAC CAAGGCTTCA TTGATGCTGC TGTCTTTTTT 1080 TAAATTTATT TTTTTTTGGA GACAGGGTGC CCCATGCTGG AGTGCAGTGG TATTATGATC 1140 ACGGTTTACC TCAAACTCCT GGGCTCAAGC AATCCTCCTA CCTCAGCCTC CTGAGTAGCT 1200 GAGACTGCAG ACATGCGCCC CCAAGCCCCA GCTATTTTTG TATTTTTAGT AGAGGTGAGG 1260 TCTCACTATG TTGCCCAGAC TGGTCTCGAA CTCCTGAGCT CAAGTGATCT TCCCATCTCA 1320 GCCTCCCAAA GTTCTGGGAT TACAGGTCTG AGCCACCACC CGGCCTGTCT CTGCCTTTTT 1380 TCTACCCCCA CCCGGGGCTT TCTGCAAGCA AGACACAGCT ATGCAAACAG 1430
|
| |
|
|
|