| Tag | Content |
|---|
EnhancerAtlas ID | HS047-12741 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr16:28514150-28515010 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr16:28514982-28514993 | GCTTCCCGCCC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr16:28514497-28514512 | TGAACTCTTGACCTC | - | 7.64 | | RARA | MA0729.1 | chr16:28514494-28514512 | TCTTGAACTCTTGACCTC | - | 6.45 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGGTTTGTTT TGAGATGGAG TCTCGCTCTG TTGCCCAGGC TGGAGTGCAG TGGCGCGATC 60
TCATCTCACT GCAACCTCCA CCTCCTGGGT TCAAGTAATT CTCCTGCCTC AGCCTCCCGA 120
GTAGCTGGGA TTACAGGCGC ACAGCACCAT ACCCGGCTAA TTTGGTATTT TTAGTAGAGG 180
TGGGGTTTCT TCATGTTGGT CAGGCTGGTC TCGAACTCCT GACCTCAGGT GATCCACCCA 240
CATCAGCCTC CCACAGTGCT GGGATTACAG TCGTGAGCCA CTGCGCTCAG CTAATTTTTG 300
TATTTTTTAG TAGAGATGGG GTTTCGCCAT GTTGGCCAGG CTGGTCTTGA ACTCTTGACC 360
TCAGGTGATC CGTGCTCCTC AGCCTCCCAA CGTGCTGGGA TTACAGGCAT GAGCCACCAC 420
GCCTGGCAGT TTATTTATTT TTCTGAGACA GGGTTTCCCT CTGTTCTCCA TCCTGGAGTC 480
CAGGATCATA ACTCACTGCA GCCTCCAACT CCTGAGCTCA AGCAATCCTC CCATGTCAGC 540
CTCCTGAGTA GCTGGGACCA AAGGTGTACA CCACCATGCC TGGCTAACTC TTAAATTTTT 600
TTTTGTAGAG ACAAAGTTTC ACTATGTTGC CCAGACTGGT CTTGAACTCC TGGCCTCAAG 660
CAGTCCTTCC ACCTGGGCCT CCCAAAGTGC TGGGTTTATA GGTGTAAGTC ACCATGCCTG 720
TCTTTCATCT CTATGTCCAA TGACATATTC AGCCTTATCC AGGTTCTATC CCCAATGCAT 780
CTCCAGCTCA ATCTCCAGCC TCATCTTGCA CCCTGGCCCC AGCCTATCAC AAGCTTCCCG 840
CCCCACTCCA CCAGCCCTCA 860
|
