| Tag | Content |
|---|
EnhancerAtlas ID | HS098-24057 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:41773110-41774560 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr17:41774026-41774038 | GCTATTTATAGC | - | 6.32 | | MEF2B | MA0660.1 | chr17:41774026-41774038 | GCTATTTATAGC | - | 7.22 | | POU4F2 | MA0683.1 | chr17:41774511-41774527 | GTGCATAATAAATGTG | + | 6.77 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTACAGGGAA AATCACAATC CCAGAAGATA AGACAAAGAA CAGTAAAAGG TGGCTTTTGA 60
GGCAGTGAGT TCTACCTGAA GGTGGGAACA GCCCAGAGTG TCTGGGGACA GAGTGGTAAA 120
TTCTAATCAA GCCTTCCCAT GGCTTTGTGG ATGAGGATGA GTTTCTACCC TGAAGCTCGG 180
CCTGTTCAGC CATAAAATCA GGATAATGGT GGCTGTGCCT CCTTAGAGTA GAATGAGAAT 240
CAGAGCAGAA CAAGGGAAAG CTGCAGTGAC TTGTCAGGTG TCAACCTTCA GCATGATGGG 300
AGAGCCATGG GACCCTTCCC CTTTCCCTAA GAGAGCCAGC CCTCACAGCA GGCCTGGGAT 360
CCAATGCCCA GCACCCAGCT GGGAGCCCAG GGACCTTGGC CAAAATCTGG TTCTGCTTCA 420
ACTTGGTGCC CGGCCTTTGT CAAGTCACTT CCTCATTTGC AAACTGGGAG AGTTTGGATG 480
AAACTATTGA ATGAAATTAT TTTGGGGGTT TCTTTCTGGC TCTCACAGTC CTCGCATGCT 540
CACCATGTTC CCTTCAATTT CATTAGCACA GCCCAACAAA GGGTTAAGCA GTGGCAGTTC 600
CTCTCGTTCT TTGGTTAGGA CAGGAAGGTC AGGGGTGAGG CCAATACAAG AGGTAGCCGC 660
CACAGCTGAT GCTGGAAATG ACAATAGTTC TTTCCTAGAC TCATATTTGT CCCCTCTCCC 720
TGAAGCTTTG CCTGCAGTGC CCTTGTAAAG AAGTTGGCAA GAAGCAGGAG TGAGGCTCAG 780
CCCCTCTCTG AAATGGATAC GCCGGTTGCT CCCCCTCATG GCTGGTCTCA TTTGCCTTCT 840
TCATTTTTAG ACACATTCCA AACTTTTCAG CAAATTATAG TGTTTGCCAA CTGGCCGTCT 900
GGGGCCCAGG AGAGATGCTA TTTATAGCGA TGCTGGGATG CTGCCATCCC AGAGCAGCCT 960
GGTAAGAAAC GGAGCCAGAG TGCCTGGGAG TGGCGTCCTG CACCCTGGGG AGAGGCCAGG 1020
GCCCTGGAGC AGGGTGGCAA AGCTGGTGGC CCGTGGCAAG GACCACTGGC ACATCCCCTG 1080
CCTGCCTGGG CCCTGGGGTC TGTGCCCATA CCCCACACGG GGGGCTGCTT CCGTGCTCCT 1140
TGGAGAGACG ATGGTGCTGT GGGGCCACTG AGCACAGTAA AGGCTAAGAC CCACCATAGG 1200
TCAGCCCTTG CTCATGCTGA CTGTTGCCCC ATTTCCCTTC ATTCTCTCAC TCGTTCATTC 1260
CTCAGAATCT GCATCCTGGT TTTGTCACTA CCTGGAGTTG TAAAGATACC ACCAAGCTCA 1320
CCTTGTGGTG TGAGCCTTGA TTTTCCCCAT CTGTGTAAAG GGTGGATCTG AGCTCCAAAG 1380
TTCCTTCTAG TCATATGCAG AGTGCATAAT AAATGTGTTT GTATTCCCAC TGTGCTCAGT 1440
GGGCACTGGG 1450
|
