| Tag | Content |
|---|
EnhancerAtlas ID | HS182-09455 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr17:41773360-41774490 |
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 | CAAGGGAAAG CTGCAGTGAC TTGTCAGGTG TCAACCTTCA GCATGATGGG AGAGCCATGG 60
GACCCTTCCC CTTTCCCTAA GAGAGCCAGC CCTCACAGCA GGCCTGGGAT CCAATGCCCA 120
GCACCCAGCT GGGAGCCCAG GGACCTTGGC CAAAATCTGG TTCTGCTTCA ACTTGGTGCC 180
CGGCCTTTGT CAAGTCACTT CCTCATTTGC AAACTGGGAG AGTTTGGATG AAACTATTGA 240
ATGAAATTAT TTTGGGGGTT TCTTTCTGGC TCTCACAGTC CTCGCATGCT CACCATGTTC 300
CCTTCAATTT CATTAGCACA GCCCAACAAA GGGTTAAGCA GTGGCAGTTC CTCTCGTTCT 360
TTGGTTAGGA CAGGAAGGTC AGGGGTGAGG CCAATACAAG AGGTAGCCGC CACAGCTGAT 420
GCTGGAAATG ACAATAGTTC TTTCCTAGAC TCATATTTGT CCCCTCTCCC TGAAGCTTTG 480
CCTGCAGTGC CCTTGTAAAG AAGTTGGCAA GAAGCAGGAG TGAGGCTCAG CCCCTCTCTG 540
AAATGGATAC GCCGGTTGCT CCCCCTCATG GCTGGTCTCA TTTGCCTTCT TCATTTTTAG 600
ACACATTCCA AACTTTTCAG CAAATTATAG TGTTTGCCAA CTGGCCGTCT GGGGCCCAGG 660
AGAGATGCTA TTTATAGCGA TGCTGGGATG CTGCCATCCC AGAGCAGCCT GGTAAGAAAC 720
GGAGCCAGAG TGCCTGGGAG TGGCGTCCTG CACCCTGGGG AGAGGCCAGG GCCCTGGAGC 780
AGGGTGGCAA AGCTGGTGGC CCGTGGCAAG GACCACTGGC ACATCCCCTG CCTGCCTGGG 840
CCCTGGGGTC TGTGCCCATA CCCCACACGG GGGGCTGCTT CCGTGCTCCT TGGAGAGACG 900
ATGGTGCTGT GGGGCCACTG AGCACAGTAA AGGCTAAGAC CCACCATAGG TCAGCCCTTG 960
CTCATGCTGA CTGTTGCCCC ATTTCCCTTC ATTCTCTCAC TCGTTCATTC CTCAGAATCT 1020
GCATCCTGGT TTTGTCACTA CCTGGAGTTG TAAAGATACC ACCAAGCTCA CCTTGTGGTG 1080
TGAGCCTTGA TTTTCCCCAT CTGTGTAAAG GGTGGATCTG AGCTCCAAAG 1130
|
