| Tag | Content |
|---|
EnhancerAtlas ID | HS042-23504 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr2:899800-900900 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr2:900811-900822 | GGGCGGGAAGG | + | 6.62 | | Mecom | MA0029.1 | chr2:899933-899947 | ATTTATCTTATCTC | - | 6.36 | | ZNF263 | MA0528.1 | chr2:900412-900433 | AGAGGAGGGTTAGGAAAAGGA | + | 6.26 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAACCTGTTA ATTCTGCATT TATAGTGATT TGTAATAGTT TTTCTAATTA AGGCAAACTA 60
AACGAAATCA GTTAATAACG AAGTAGATTT TATCCCTCAT GTACGCTAAT ATAGACTAAC 120
ATGAAATCCC ATAATTTATC TTATCTCAAA GCACATTTTT ATACCAGGCA GCTGATTTGG 180
TTTCTGCCCT CAGTCTATTC TCTCTCACAC AGACTCCCCT TTTCTTTTTC TCTGTTTCTG 240
TTTTTCCTGT CCTTCGCACC CTCAGCAGGG AGCTCAACTT CCTGGCACTA TTCTCACACA 300
CATGTCAGGT GTAAACATCT TTATGGGGGA AACAGGCTCT GGCTGTCTCA CAAAGCTTTA 360
GTTGTCATGC ACATGTAACA CTTTCATTCA CTTCTTAAAG GTGATTTACA TGAGCCTCGC 420
ACAGCTGAGA CGTATTTCGC TGCTTACTAA ACCTTGAATG ATGGTGCGTC ATTCTCATTA 480
AAACAAGGAA GCACAGGAAG GTGGAAGTAT AAATTTTTGT GAGTGTTTCT GGCCCACTAT 540
GAAAGTGCGA CAGCGGGCAT GGCTGTCTAG GCCTCCCTGG CAGCACTGGT GTGGGGGCTC 600
CCAGGAAGGA GTAGAGGAGG GTTAGGAAAA GGATGGGAGG GCCACGGGCC TGGCAGCTGA 660
GCAGCACCTG GGCCCTCACA GCTCAGATTG CAGAGCAAAG AGGGAGCCAC GTGTGGAGGG 720
TGGGGAACAT GGAGCGAGAA GGGGAGGGAA GCACAAAAGG GAGCACAAGA GGAGAGAATG 780
GAGGGGAGCA TGGGAGGGAG CATAGAAGGG GGCATAGAGG AAACACAAAG GGAGCACTGG 840
GGAGAGCATG AGAGGAACAG GGGAAGCACA GGCGAGGTAG CACAGGGGGG AGCACTAAGA 900
GAGCACACCG CGGAGCTGCC TCCACCCAGG CCTGGCATGA GCAGGGTTGA CCCCAGAGCC 960
CAGACCCTTC CCCCAGGAGC ACAGGGAACA GGCAGTGTTC CCCCACAGTG GGGGCGGGAA 1020
GGAGAGTCCA AGGGCCAAGG AAGGGCTGAT GGTCCATTTC CTGTGGAATT GCGCCAACCT 1080
GATGGCATCC ATAAGGCACA 1100
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