| Tag | Content |
|---|
EnhancerAtlas ID | HS047-18366 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr2:11495230-11496410 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr2:11496393-11496404 | AAGAGGATTAA | + | 6.14 | | Foxd3 | MA0041.1 | chr2:11495476-11495488 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr2:11495480-11495492 | AAACAAACAAAC | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGAGGCCGAG GTGGGCAGAT CACTTGAGGT CAGGAGTTCC GAGACCAGCC TGGCCAACAT 60
GGTGAAACAT CATCTCCACT AAAAACACAA TTAGCCAGGT GTGGTGGCAG GCACCTGTAA 120
TCCCAACTAC TCAGGAGGCT GAGGCAGGGG AATCGCTTGA ACCCAGGGGG CAGAAGTTTC 180
AGTGAGCCAA GATCGTGCCA CTGCATTCCA GCCTGAGTGA CAGAGTAAAA CTGTGTCTCA 240
AAAAAAAAAC AAACAAACAA ACAATAAAAA GGCAAGGTCT GAGCTTCGTG ATCTGGGGAG 300
GGAAATGAGA CATATGCACA GAGGCTGGCC AGGAGTGAGT GCGTGCTCAG TGTATTTATA 360
GCCTGAACAA ATGATTGAAT GAATGAACAG AAGGACATAA GCACGAGCAA GCCACGTGGT 420
ACAGAAGAAA GAACACAGGC TTGTGGCATC CCAGCTCCCC CACTTCCAGC TGTGTATGAG 480
TCTGGAGAGT TCCGCTAGCT TCTAGAGCCA CTGTCCACCC TGCTCTGCGC CCCAGGGGCT 540
GACCTCTATG GACTGCCTAC TCTGGGCTCT CTGTGGTCTA TCTTCTGGTT GAGCTCTGCC 600
CAAAGGGAGA GCTGGAAAGA GATTGGGGGT GAGGACAGGG TTTTAACCCC CTAAATCCCT 660
GGAAAGAGAT TGGGGGTGAG GACAAGGTTT TAACCCCCTA AATCCCTGGA AAGAGATTGG 720
GGGTGAGGAC AGGGTTTCTT CCCCTCTGCC CCAGCTTGAC CTCTGGCAGC AGCTCTGCAC 780
CTCAATCCCT GCAGCTCCGC GGACTGCATT CCATTGCTCA CTGGGCCTCA GGGAGGTTAT 840
GTCCTCTCTC TGCCCTCCTG ACCTCAGCTT CTCACTGTCG CTGGGGTCTC AGTGCCTCAA 900
CATTTCTTGT CTTCCTTTAA TTCTGTCTAC ACCTCTGGAA AGAGCTCCTC TATGGAAACC 960
ATCTGAGTTA GTTCTATTTC CTGAAGAGAC CCAACTTATT CAGTAAATTA GAGGCAATCA 1020
CAGAACTCGT CATAGTCAGA TTCCTCCACT ATGAAATGGA AATAGTAGCA ATACTTAGTA 1080
TCTAGCACAG TTCAGTGCCT GGACATTGGC CCTCATACAT GTTGGCTGCT TAAATTAGTG 1140
AATACCTGAA TGAATTAATG GCTAAGAGGA TTAATGATGA 1180
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