| Tag | Content |
|---|
EnhancerAtlas ID | HS164-04975 |
Organism | Homo sapiens |
Tissue/cell | Raji |
Coordinate | chr16:71969420-71970360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr16:71970324-71970339 | TGAACTCCTGACCTC | - | 6.22 | | ONECUT1 | MA0679.1 | chr16:71969678-71969692 | TAAAAATCAATAAT | + | 6.77 | | ONECUT2 | MA0756.1 | chr16:71969678-71969692 | TAAAAATCAATAAT | + | 6.91 | | ONECUT3 | MA0757.1 | chr16:71969678-71969692 | TAAAAATCAATAAT | + | 7.34 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCTAAACATA GACAGCACAG TCACTGTTGC TTGTCTGAGA GATTAGCTAG GTCTCTCCCT 60
GCTCAAGTGT GATGAACGCA GCTGATGTCT GTGGGCAAAG CACACTGCCA GGCATTTATC 120
AGATCTCACT TGGACAAATG GGTTATGGTC TTAGTTCAGG TCTGTAGTCT TCAGAAATGC 180
TGCTTACAAA AAAGTTATCT TCAAACAACT TCCATTGGAT ACATTTATTC TTTTTCTTGG 240
AGATCATAAA CTGTCACTTA AAAATCAATA ATACAAAAGT TTCTTTCTTT GAGACAGGGT 300
CGCGCTCTGT TGCCCAGGCT GGAGTGCAGT GGTGCGATCA TAGCTCACTG CAGCCTCAAC 360
CTCCCAGGCT CAGGCTCAAG CAGTCCTCCT ACCTCAGCCT CCCAAGTAGC AGGGACCACG 420
AGCACATGCC ACCATGCCCG GCTAAGTTTT GTATTTTTTG TAGAGACAGG GTTTTGACAT 480
TTTGCCCAGG CTAGTCTTGA ACTCCTGGCT TCAAGTGATC TGCCTACCTC AGCCTCCCAA 540
GGTGCTGGGA TTACAGGCGT GAGCCACCAT GCCCAGCAAA AATTTCTAAA TTAGTTATCA 600
AGCCTGAGAA TGAAAAAAAA AATACTATGT TTGGCTTAAG ATATAAATAT ATTTTCTTCT 660
GAGTGTAATC ATCTGTATTT TTTTTTCTTT TCTTTTTTTT TTTTTGAGAC AGAGTTTCAC 720
TCTTGTCACC CAGGCTGGAG TGTAGTGGTG CCATCTTGGC TCACTGCAAC CTCTGCCTCC 780
CAGGTTCAAG CAATTCTGCC CCAGTCTCCC GAGTAGCTGG GACTATAGGA GCCCGCCACC 840
ATGCCCAGCT GATTTTTGTA TTTTTAGTAG AGACAGGGTT TCGCCATGTT GGCCAGGCTG 900
GTCTTGAACT CCTGACCTCA GGTGATCAAC CCATCTTGGC 940
|
