| Tag | Content |
|---|
EnhancerAtlas ID | HS108-15980 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr16:89852700-89853750 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr16:89853526-89853541 | TGCTATTTTTGAAAA | - | 6.03 | | Nr2f6(var.2) | MA0728.1 | chr16:89852809-89852824 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCTGCCTCAG CCTCCTGAGT AGCTGGGATT ACAGGTGTGC ACCACCATGC CTGGCTAATT 60
TTGTGTTTTT AGTAGAGACA GGGTTTCATC GTGTTGGCCA GGCTACTCTT GAACTCCTGA 120
CCTCAGGTGA TACCTTGGCC TCCCAAAGTG CTGGGATTAC AGACATGAGC CACCACGTCT 180
GACCTAGCTA ATTTTTGTCT TTTTAGTAGA GATGAGGTTT TGCCATGTTG GCCAGGCTGG 240
TCTCAAACTC CTGACCTCAA GTGATCCACC TGCCTCGGCC TTCCAAAGTG CTGGGATTAC 300
AGGCATGAAC TATCACACCT GACCATGTGT AGATTCTTTT GAATGTTATC ATCATGCAGA 360
CAGACCCAAA AAGCCATTAG ATAAAAAGCG GAAAATGCTG ATAACGCTTG TCAAATGTCT 420
CTGAGAGGGA CAGAGTCACG GAAAAACAAA GCTCAGAGAC ATGAACTGTC TGTGCCAAAT 480
ACCAGGAAAG CAGCTCAATA CTTGTCAGTT AAAAATTTAA ATAAAACCTG AGACCACTCA 540
AGGGTTCCCT TCTCAAAACA TCAGCACCCA GTTTCAACCT GAAATTCTCC CGCCAAGCAC 600
ACCATGTCTT ATCACCCTCC ATTCAGCCAT CCACAACACA ACTGCTCCTG TCTCTTGGCA 660
ACGTTCACTC AATTAACAGT GAGCCAGATG ATCACTGGCC GCAGCAGGAA CAGTCCAGAC 720
CCGTCGCCAA AGGCATTTCT GTAAAGCATC TAAGTGACAC GCGCAAGCCA GACCTGGGGT 780
CACAGCAGCC ATTGTTAGAG TTGCTGAGAT AAAAGGCAGT TCTGTTTGCT ATTTTTGAAA 840
AAATTACACT TAATGGCTGG GTGCAGTGGC TCAATCCGGT AATTCCAACA CTTTGGGAGG 900
TTGAGGCAGG AAGATCACTT CAGCCCAGGA GGTCAAGACC AGCCAGGACG GCCGGGCGCG 960
GTGGCTAGCG CCTGTGATCC CAACACTTTG GGAGGCTGAG GCGGGCAGAT CACGAGTTCA 1020
GGAGATCGAG ACCATCCTGG CTAACCCGGT 1050
|
