Tag | Content |
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EnhancerAtlas ID | HS047-18242 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:636550-637250 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr2:637095-637106 | GGGCGGGAAGA | + | 6.14 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I000636 | chr2 | 636179 | 637357 |
|
Enhancer Sequence | GCAGGCCTCG GGTTCCATCG CAGCAGCGTG GCCTGATGAC TCCATTTTGT CGCTGCGGAG 60 GAGCCGCACC GAGTCCACAG CGCCAGTGCG GGGGAGCCGC GCCGGGGAAG AGGGAGGAGG 120 CGCGTCCACA GCAGCCTCGT GTCTCCACAT GGGACGTTTC CTCGGCGGGG ACCCGGCGCG 180 CCCAGGGGCT CAGGCTCGCT CAGGCCTACG GAGGCGGGTG TATCCGCGTC CGGCCCGACT 240 TGTGAGGAAA CAGCACACGT GAAGCGAGCG GAGTCGGCGC AGCCTGGAAC AGGGTGAATC 300 CGCAGAGTCC TCGGCCGCGC ATGGCGGCTC TGTCAGCTCC AGGGACACAG GGACCGTCCC 360 CGGGCCCATC AGCGCAATCG GGAGGGCGTC CGTGTGCCCA CAGGCCCAGC TACACCTCCA 420 CAAAGCTGGG AAAGACGAAC ACGGGCCACC CTCAGCCACC TGCCCGGACC GCTGCGAGGC 480 CCACGGGAGG GAAGACGCGC CCTGGCACGC GGTGTGGTAA CCGCCCTTGG ACGCGGCGGC 540 GCTTTGGGCG GGAAGAACCG CGAATTCCAG AACATTTGGG ATCATTTGTT AAAAGAAAAA 600 TCCTCGGGCG CCACCTAGCG CTGACATGCT GCCTAACTCT TCTCAGCCCT CATTTTAGAG 660 AACGGAAAAT GAAGCCCAAG TTATTGACTA TAAAATGGGA 700
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