| Tag | Content |
|---|
EnhancerAtlas ID | HS047-00808 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr1:29044500-29045650 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr1:29045568-29045583 | AACGCTGAGTCATGC | - | 6.2 |
| | | 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 |
| GH01I028718 | chr1 | 29045242 | 29045713 |
| Enhancer Sequence | TTTTCCTGGT CTTCCAATAG CCTGTCATTA TTGTTAGATA TTATGGCACC TGTTGTTGAA 60
TGTAGGTTCC CTTACAGCCC TGGTCTAGAT GATCCTAGAT GGGGTGAGAC ATATGCAAGC 120
CATTGGTATG TGCATAAGCA GTTGCAATGA ACCTTAGGCT GACTTGGTAG TAGGCATTTG 180
TCTTTCTGTT CATGCATTGA ATAAACATTT TTAAGAACCA TCTATGTGCC AGGCTTTGTG 240
CTAGGCACTG ACAGTAGAGA GATGAAGACA TAGTCCTTGC ACTTAAGGAA TTCATACTCC 300
AGATGTCTGG AGTTAAGAAA TACATATTTC AGCCAGGCAT GGTGGCTCAC ACCTAGAATC 360
CCAGCACTTT CAGAAGCTGA GGCAGAATTG CTTGAGGCCA AGAGTTTAAG ACTAGCCTGG 420
TCAACATAGC CAGACCCCAT CTCTATAAAA AAATGTAAAA ATTAGTCAAG TCTTGTGGCT 480
CGCACTTGTA GACACAATTA CTCAGGATGC TGAGGCAAGA GGATTTTGCT TGGGCCTAGG 540
AGTTCAAGGC TGTAGTGAGC TATGACTTTG CCACTGTACT CTAGCCCAGG TAACAGGGCA 600
ACATCCCCAG CTCAGAAAAC CAAAACTACA CATTTCATTA TAATTGTTTT TTTTTGTAAT 660
TTTATGTATT TTATGCATTG AAAAACATTA TTTAAGAATT GGTTCATAGG TTTCAGCAGA 720
CTGCCAAAGG CACAAACAAG CAGCTCTCCT TTACTGAGGT ACTGAAACAG ATCCTACTGC 780
GTAAGTGCTG TGTGTGATAG GGCTATTGGC TAGGAGCTGA GAGAACAAAG CATGAAGTGC 840
CTAACCCAGC TTAGCGGTGT AGAGGTGGGG TCAGCAAATA AGGGAGATCT TCCTGGAGAA 900
GGCATATACC TAAGCTGATT TAGGAGAGAC CACTTTTGGC TAGGTTTATT GTACTACTTG 960
ATTTTCAAGT AATTGGGCTT ATTTATTCTA GAGAAAAAGT CTTCAGTCTC TTGCTTCTGC 1020
CTGCAAAGCA AGGCAGAGTC AGCAACATGG GCAGTCTCCC CACTGGAGAA CGCTGAGTCA 1080
TGCATGGGCT TCTCCAAGTT TCCATCAGAT GGGATCCAGT GTTGAATCCA GTGCAGGACT 1140
GGAGTCTAGC 1150
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