| Tag | Content |
|---|
EnhancerAtlas ID | HS094-16787 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr17:41773390-41774360 |
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 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCAACCTTCA GCATGATGGG AGAGCCATGG GACCCTTCCC CTTTCCCTAA GAGAGCCAGC 60
CCTCACAGCA GGCCTGGGAT CCAATGCCCA GCACCCAGCT GGGAGCCCAG GGACCTTGGC 120
CAAAATCTGG TTCTGCTTCA ACTTGGTGCC CGGCCTTTGT CAAGTCACTT CCTCATTTGC 180
AAACTGGGAG AGTTTGGATG AAACTATTGA ATGAAATTAT TTTGGGGGTT TCTTTCTGGC 240
TCTCACAGTC CTCGCATGCT CACCATGTTC CCTTCAATTT CATTAGCACA GCCCAACAAA 300
GGGTTAAGCA GTGGCAGTTC CTCTCGTTCT TTGGTTAGGA CAGGAAGGTC AGGGGTGAGG 360
CCAATACAAG AGGTAGCCGC CACAGCTGAT GCTGGAAATG ACAATAGTTC TTTCCTAGAC 420
TCATATTTGT CCCCTCTCCC TGAAGCTTTG CCTGCAGTGC CCTTGTAAAG AAGTTGGCAA 480
GAAGCAGGAG TGAGGCTCAG CCCCTCTCTG AAATGGATAC GCCGGTTGCT CCCCCTCATG 540
GCTGGTCTCA TTTGCCTTCT TCATTTTTAG ACACATTCCA AACTTTTCAG CAAATTATAG 600
TGTTTGCCAA CTGGCCGTCT GGGGCCCAGG AGAGATGCTA TTTATAGCGA TGCTGGGATG 660
CTGCCATCCC AGAGCAGCCT GGTAAGAAAC GGAGCCAGAG TGCCTGGGAG TGGCGTCCTG 720
CACCCTGGGG AGAGGCCAGG GCCCTGGAGC AGGGTGGCAA AGCTGGTGGC CCGTGGCAAG 780
GACCACTGGC ACATCCCCTG CCTGCCTGGG CCCTGGGGTC TGTGCCCATA CCCCACACGG 840
GGGGCTGCTT CCGTGCTCCT TGGAGAGACG ATGGTGCTGT GGGGCCACTG AGCACAGTAA 900
AGGCTAAGAC CCACCATAGG TCAGCCCTTG CTCATGCTGA CTGTTGCCCC ATTTCCCTTC 960
ATTCTCTCAC 970
|
