| Tag | Content |
|---|
EnhancerAtlas ID | HS182-05487 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr12:120979880-120980900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr12:120980740-120980752 | TTCTGTTTACAT | - | 6.92 | | FOXP2 | MA0593.1 | chr12:120980741-120980752 | TCTGTTTACAT | - | 6.02 | | Foxa2 | MA0047.2 | chr12:120980743-120980755 | TGTTTACATTGC | + | 6.07 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGATGGTCTT GATCTCCTGA CCTCGTGATC CACCCGCCTC AGCATCCCAA AGTGCTGGGA 60
TTACAGGCGT GAGCCACCGT GCCTGGCCTT TTTCTTTTTT TGAGACAGAG GCTCACTCTG 120
TAGCCCAGGG TGGAGAGCAG TGGTGCCATC ATAGCACACC GCAGCCTCAA CCTTGGCTTA 180
AGCAATCCTT CCAACTCAGC CTCTCAGCTA GGACTGCAGG TGTGTGCCAC CACATTGGGC 240
TAATTTTTAA ATTTTTTGTA GAGATGGGGT CTTGCTATGT TGCCCAGGCT GGTCGCAAAC 300
TCGTGGACTC AAGTGATCCT CTTGCTTTGG CTTCCCAAAG TGTTGAGACA ACCGGCATGA 360
GCCACCAAGT CCAGCGCTGA AACTTTGCTT TCTAATTGTT ACTACTAGTG CCATGTTTGA 420
CACTAACTGT TGCTAACTGA AGTAATAGGT AAAAGTTTAG TTTTTAAGTT CTAACTTTAT 480
TTATTTGTTT TTTGAGACAG AGTCTCACTC TGCTGCCCAG GCTGGAGTGC AGTGGCGTGA 540
TTTCAGCTCA CTGCAACCTC TGCCTCCCGG GTTCAAATGA TTCTCATGCC TTAGCCTCCC 600
AAGTAGCTGG GATTACAGGC GTGTGGCACC ACACCTGGCT AATGTTTGTA TTTCTAGTAA 660
AGATGGGGCT TCACCATGTT GGCCAGGCTG GTCTCGAACT TCTGGCCTCA TGTGATCTGC 720
CTGCCTTGGC CTCCCAAAGT GCTGGGATTA CAGGGAGCCA CCATGCCTGG CCTTAAATTG 780
TAACTAAGGT AAGGGTCACT GTCCGTAAGC AGGATTTAAG GGTAACTGGT AGGAGTGAAC 840
CTAGCCTGTT TCTGTGACTG TTCTGTTTAC ATTGCTGCCA TTTCACATGG TTTAGATTGA 900
CTCCCAGGTT TTAGGTGGTC AGGTTTGGAG AGAATGACAT CTCATTTATA CAGTGAGGTT 960
GACAGACTAT GGGCGTGAAG TGGTTGCTTT CAAAATTTGG TCTCTGATTT ATTAACTTAC 1020
|
