| Tag | Content |
|---|
EnhancerAtlas ID | HS176-15737 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr16:89852750-89853880 |
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 | CTGGCTAATT TTGTGTTTTT AGTAGAGACA GGGTTTCATC GTGTTGGCCA GGCTACTCTT 60
GAACTCCTGA CCTCAGGTGA TACCTTGGCC TCCCAAAGTG CTGGGATTAC AGACATGAGC 120
CACCACGTCT GACCTAGCTA ATTTTTGTCT TTTTAGTAGA GATGAGGTTT TGCCATGTTG 180
GCCAGGCTGG TCTCAAACTC CTGACCTCAA GTGATCCACC TGCCTCGGCC TTCCAAAGTG 240
CTGGGATTAC AGGCATGAAC TATCACACCT GACCATGTGT AGATTCTTTT GAATGTTATC 300
ATCATGCAGA CAGACCCAAA AAGCCATTAG ATAAAAAGCG GAAAATGCTG ATAACGCTTG 360
TCAAATGTCT CTGAGAGGGA CAGAGTCACG GAAAAACAAA GCTCAGAGAC ATGAACTGTC 420
TGTGCCAAAT ACCAGGAAAG CAGCTCAATA CTTGTCAGTT AAAAATTTAA ATAAAACCTG 480
AGACCACTCA AGGGTTCCCT TCTCAAAACA TCAGCACCCA GTTTCAACCT GAAATTCTCC 540
CGCCAAGCAC ACCATGTCTT ATCACCCTCC ATTCAGCCAT CCACAACACA ACTGCTCCTG 600
TCTCTTGGCA ACGTTCACTC AATTAACAGT GAGCCAGATG ATCACTGGCC GCAGCAGGAA 660
CAGTCCAGAC CCGTCGCCAA AGGCATTTCT GTAAAGCATC TAAGTGACAC GCGCAAGCCA 720
GACCTGGGGT CACAGCAGCC ATTGTTAGAG TTGCTGAGAT AAAAGGCAGT TCTGTTTGCT 780
ATTTTTGAAA AAATTACACT TAATGGCTGG GTGCAGTGGC TCAATCCGGT AATTCCAACA 840
CTTTGGGAGG TTGAGGCAGG AAGATCACTT CAGCCCAGGA GGTCAAGACC AGCCAGGACG 900
GCCGGGCGCG GTGGCTAGCG CCTGTGATCC CAACACTTTG GGAGGCTGAG GCGGGCAGAT 960
CACGAGTTCA GGAGATCGAG ACCATCCTGG CTAACCCGGT GAAACCCTGT CTCTACTAAA 1020
AATACAAAAA ATTAGCCGTG TGTGGTGGCA GGCGCCTGTA GTCCCAGCTA CTCAGGAGGC 1080
TGTGGCAGGA GAATGGCGTG AACCCGGGAG GTGGTTACCG TGAGCCAAGG 1130
|
