| Tag | Content |
|---|
EnhancerAtlas ID | HS047-18831 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr2:42812520-42813640 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr2:42813501-42813511 | ACCACTTGAG | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCTGGCTGAA AAGTGGAAAT TATTAAAAAG AAAAACATTG TAAGTTGAGT TCAGTAACAA 60
TATGAAAGAC CAAATGATTC TTTTTTCTTT CTTTTCTTTT TTTTTTTTTT TTTTGAGACA 120
GTCTCACTCT GTCGCCCAGG CCGGAGTGCA GTGGTGCAAT CTCAGCTCAC TGCAACCTCC 180
GCCTCGTGGG TTCAAGTGAT TCGCCTGCCT CAGCCTTCTG AGTAGCTGGA ACTACAGATG 240
TGTGCCACCA CGCCTGGTTA ATTTTTGTAT TTTTATAGAG ACCGGGTTTC ACCGTGTTGG 300
CCAGGATGGT CTTGAACTTC CAACCTCAAG TGATCCACCT GCCTTGGCCT CCCAAAGTGC 360
TCGGATTAGA GGCATGAGCC ACTTTGCGTG GCCCCATCCT GTATTTTATT TTATTTATTT 420
GGTTATGTAT AATTACAGTT TTACCTACAA AGGAGGGTGA GATAGGAGAA TCACTTGAGT 480
CCAGTATTTC AGGGTTGGAA TGAGCTATGA TTGAGCAATT GCATTCCAGC CTGGGCAATA 540
GAGTGACACC TGTGTCTCTT TAAAAAAAAA TAAATTATAA ACAAGATGAA TAACTTCCTG 600
ACAAATAAAA AGAAAATTTA GGGCCAGGCG CAGTGGCTCA TGCCTCTAAT CCCAGCACTT 660
TGGGAGGCCG AGGTGGATGG ATCACTGGAG GTCAGGAGTT CGGCCTGACC AACGTGGTGA 720
AACCCTTTGT CTACTAAGAA TGCAAAATTA ACTGGGCATG GCAGCACATG CCTGTAATTC 780
CAGCTGCTTG GGAGGCTGAG GCAGAATTGC TTGAACCCGG AAGGTGGAGG TTGTAGTGAG 840
CTGAGACTGT ACCATTGCAC TCCAGCCCGG ACAACAGGAG TGAAACTCCA TCTCAAAAGA 900
AAAAAAAAAA AAAGAAAATT TAGGCCAGGG GCAGTGGCTT ACGCCTGTAA TCCAAGCACT 960
TTTGGAGGCC AAGGTAGGAG GACCACTTGA GTCCAGGAGT TGGAGACTAG CCTGGGCAAC 1020
ACAGCGAGAC CTCATATCTA AAAGTGAAAA AAAAAAAAAA GGAAATTTCA AGAAACCGGT 1080
ACAAAGAAGG AAGGAAAACA CACACACACA CACACACACA 1120
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