Tag | Content |
---|
EnhancerAtlas ID | HS007-06690 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr16:89852740-89854080 |
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: 2 | Chromosome | Start | End |
chr16 | 89854018 | 89854068 | chr16 | 89852981 | 89853039 |
|
Enhancer Sequence | ACCACCATGC CTGGCTAATT TTGTGTTTTT AGTAGAGACA GGGTTTCATC GTGTTGGCCA 60 GGCTACTCTT GAACTCCTGA CCTCAGGTGA TACCTTGGCC TCCCAAAGTG CTGGGATTAC 120 AGACATGAGC CACCACGTCT GACCTAGCTA ATTTTTGTCT TTTTAGTAGA GATGAGGTTT 180 TGCCATGTTG GCCAGGCTGG TCTCAAACTC CTGACCTCAA GTGATCCACC TGCCTCGGCC 240 TTCCAAAGTG CTGGGATTAC AGGCATGAAC TATCACACCT GACCATGTGT AGATTCTTTT 300 GAATGTTATC ATCATGCAGA CAGACCCAAA AAGCCATTAG ATAAAAAGCG GAAAATGCTG 360 ATAACGCTTG TCAAATGTCT CTGAGAGGGA CAGAGTCACG GAAAAACAAA GCTCAGAGAC 420 ATGAACTGTC TGTGCCAAAT ACCAGGAAAG CAGCTCAATA CTTGTCAGTT AAAAATTTAA 480 ATAAAACCTG AGACCACTCA AGGGTTCCCT TCTCAAAACA TCAGCACCCA GTTTCAACCT 540 GAAATTCTCC CGCCAAGCAC ACCATGTCTT ATCACCCTCC ATTCAGCCAT CCACAACACA 600 ACTGCTCCTG TCTCTTGGCA ACGTTCACTC AATTAACAGT GAGCCAGATG ATCACTGGCC 660 GCAGCAGGAA CAGTCCAGAC CCGTCGCCAA AGGCATTTCT GTAAAGCATC TAAGTGACAC 720 GCGCAAGCCA GACCTGGGGT CACAGCAGCC ATTGTTAGAG TTGCTGAGAT AAAAGGCAGT 780 TCTGTTTGCT ATTTTTGAAA AAATTACACT TAATGGCTGG GTGCAGTGGC TCAATCCGGT 840 AATTCCAACA CTTTGGGAGG TTGAGGCAGG AAGATCACTT CAGCCCAGGA GGTCAAGACC 900 AGCCAGGACG GCCGGGCGCG GTGGCTAGCG CCTGTGATCC CAACACTTTG GGAGGCTGAG 960 GCGGGCAGAT CACGAGTTCA GGAGATCGAG ACCATCCTGG CTAACCCGGT GAAACCCTGT 1020 CTCTACTAAA AATACAAAAA ATTAGCCGTG TGTGGTGGCA GGCGCCTGTA GTCCCAGCTA 1080 CTCAGGAGGC TGTGGCAGGA GAATGGCGTG AACCCGGGAG GTGGTTACCG TGAGCCAAGG 1140 TCGCACCACT GCACTCCAGC CTGGGCAACA AGAGCGAACT CCATCTTAAA AAAACAAAAA 1200 GACCAGCCAG GGCAACATAG TGAGACACTA TGTCCACAAA AAATTTTTTA ATAATTAGCC 1260 AGGTGTGGTG ACATACACCT GCGGACTCAG CTGCTCGGGA AGTTGAGGTG GGAGGATCAT 1320 TTGAGCCTGG AAGGTTGAGA 1340
|