| Tag | Content |
|---|
EnhancerAtlas ID | HS047-02037 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr1:145713450-145714410 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:145713744-145713763 | TGGCCGCTAGAGGGCGCTG | + | 7.3 |
| | | 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 |
| GH01I145720 | chr1 | 145713284 | 145714909 |
| Enhancer Sequence | CTGGTGCAGC GGGATGGGAG GGGCGCAGGG TAGGGACCGC TTCCAAGGAG AGAGAGGACA 60
GGCGGGAGGG GCTGATGCAG CTGGTCACTC CGCTGGAGTG GCCAGACTTC GCGGTGCCTA 120
GGGCCGAGTT GAAGAAGAGC ATGTAAGTCT GTTGTGGGCC CCTCACCAGC GCTGGGGGGC 180
AGCGAGGTCA CTGGGCAAGG ATGCTCTGGG AAGTGACCTT GGTGCCCGGG AGGGGAGCAC 240
CCTGTTGTGA TGCAGGCGGG GCAGCGCGGA GCCGGCGGCG CTGATTTCGC ACTCTGGCCG 300
CTAGAGGGCG CTGCCTTTCA GCCAAAGCCG AGTGACCCCC TACCTGCCCC GCGTTGGCCC 360
GCGTCACTCC AGCCATGGGC CATCCAGCGA GCATGGGGGC TAGCCAGGGA AAGTCTAAAC 420
TAGGAGGGGA GATGAGGGGG TGCAAAGTTG GGCCTGGTGG GTCCTGGGGA CGCAGCATGT 480
ACTAGAGCGG CACCTGGCCC TCAACAGAGG GGAGAGCGGG TGGTCGTGAG AAGTCTGGGA 540
ATTTTCCGGG CCCACTACAC GCCAGGGGCG GGTCTCCCCT CTTAAAACGT TGTGAGCCCC 600
AGCGCGGGCA GGGGGGAGGG TGCCCGTGGA GTTGGCATCC TCATCTTTGA TGGTCCCCGG 660
GGCTCCTGAG CTGCGCTGGT GGCCCCAGGG CTCGGTGCCT CTCTCAGGCG ACAGCTCACA 720
GACGGCGGGA AACTCTTCCC TCCCGCACCT TCGGAGGCGG TCCTGGAGTC TTGTGGACTC 780
CTGGGTTCAA ATCCAAGCTT TGTGTGACCA GCACATTGCT GGACCTCACT CAGCCTCACA 840
TTCCTCTTGT GTTTAAAACT ACCTCATAGG AATGTGGTGA CGGTTAGATG ACACATAAAG 900
CTTTGCCAGA GGTTTTCTGG GGAGGGTGGG GACAAGAGGG CAAGGAAGAG TCTCCATTTC 960
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