| Tag | Content |
|---|
EnhancerAtlas ID | HS047-09716 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr13:114185150-114187230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr13:114186728-114186748 | CCTGTGTGGGTGGGCTGGGG | - | 6.25 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr13 | 114185514 | 114185785 | | chr13 | 114185960 | 114186309 | | chr13 | 114186326 | 114187132 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I113531 | chr13 | 114185387 | 114189142 |
|
Enhancer Sequence | AACTGAGTTT GAAAACAGGT CAGCAGCAAA GCAGCTATTA GACTTGAGTA AAGTAGGAAA 60
CACCCACCCT CACACCAAAG AAGGGTGATG GCACCACCCG CCCATCAGAC TGGGCACCAT 120
TAGAAGCTGG GTGGTGCCCA GGTTGGGAAG TGGGGTACCT TGGGCATCAT TGTTGGGATG 180
GGAATTGGAG CAACTTCCTG GCGGCCCACC AGACAGCACC TGTCATAGTG GGAGGCACCC 240
GGCTCCCTTA GTGAGCACCC ACTGCCACCA TCAGTGGACC CACAGGCTCC TTGGTCACCG 300
CAGCGCCCAA GAACCAGGAT GGCCGTGGAG TCAGTGTGAG AACCGGGACA GCCCTTGCAT 360
CTGGCTGAGC AAATGATGGT GCGTCCCGCC AGGGAGCCCT TCCTCACCTG TCCGCTGGCC 420
AGACATGCTG ATGGGAAGCT TGTCCACTCA CCTGTCCGCG GGCCAGACGT GCTGATGGGA 480
AGCTTGTCCA CTCACCTGTC CGCAGGTCAG ATGTGCTGAT GGGAAGCTTG TCCAAACACG 540
CTGAGACAGT CAGAACAGCC GTGGACACGG CGCCCCGTAT GTGCAGATCA AGAGCAGCAC 600
ACGCGTGGAC CTGCAGGTGG CACGGCGCCC TGTACATACA GATCAAGAGC AGCATGCGTG 660
TGGACCTGCA GGTGACACGG CGCCCCGTAC GTGCAGATCA AGAGCAGCAC ACGCGTGGAC 720
CTGCAGGTGG CACGGCACCC CGTACATGCA GATCAAGAGC AGCACACGCG TGTGGACCTG 780
CAGGTGGCAC GGCGCCCCGT ACGTGCAGAT CAAGAGCAGC ACGCGTGTGG ACCTGCAGGT 840
GACACGGCGC CCCGTACATG CAGATCAAGA GCAGCACGCA CGTGGACCTG CCGGTGGCAC 900
GGCGGCAAGC CGGAATCCTG AGAAACTTGT CACGGTGATT GTCTTTCAAA GAGGTCAGAG 960
TTGAGCGCAC TGTGGCTTCT GATTGGCATC TTTCTGAGCC CTCATCACTG TGCATTTAAT 1020
GGACACTGTG GGAGTCTTCT GGGAATTAGA CCTAAATCCA AACCCTGGGG ATGGTGGCTG 1080
TGGAGAGCTT GTGTAGCCGT TAGGGGCTTG GTCCTGGAGC CAGATACCTG AGTTGTCCCC 1140
AGCTCTCTGC ACTGGGCGTG TGGCCTGGAG CAGATCACCT GGTCTCTGCC CCTGTTCTCA 1200
TCTGTGACGT AGCAGTGGGG ATCGTACAGC TCTTACCAGG CTGCCATAAT AGGTGGCACA 1260
CAGTGCTCTG CACACAGTGC TCTAGGGGCT CAGGATGCAA GGGTGAGCTC AGCAGAGGAC 1320
GTTCCCCATG TGGGGAGCTG CTGTTGTGTT TTGGAGAGGC AATGAATGAA TGATGCACAA 1380
ATGAGTGGTA GACAAGACAT CCGCAGCAGG GAACCGCCCT GCGAATGATT CAAACAGGAA 1440
GAGGAGCTGG TGAGCAGCCG TGAGCCCCCA GACGCACAGG CTCTACCTTT GGAGATGTGG 1500
CTGGAATTTG AGGAATGCAG CTAAGCCTGT TGGGAGAAGA GTCTAGGGTA GGGACCTCCC 1560
AGGCAAGGGG CTCTGTGGCC TGTGTGGGTG GGCTGGGGCA GTGGAAGGGC ATGGCAGGGC 1620
AGAGAAGCCT GGGTTCCATC CCAGCGTCCA GGAGCTGATT GAGGGTCCTG ATGAGCTGTC 1680
TGGGCCTCTG TGTGGAGAGC AGATGGATCA GGAGGAGGCC ACTGGAGCTG TGGGGGAAGG 1740
GGTGGCAGCC CAGGCAGGGA CCACGGTGCT GGGCCCAGGG CCAGACGTGG GCCTGGCAGT 1800
GTGGCAAAGC TGTCAGGAGT GCGGCAGGCC TGGTCTGCTT GGCCGTGAGT CTGTCTCCGT 1860
TCCTGCCAGG GCTGCAGAAA GGGGCCTCTC TCTGAGTCGC GGACTTGGGC CCTGCAGTGA 1920
GCTCTGAAGG ACGCTGCCTC CCTCCTTCTA AGTCGCAGAC GTGGGCCCTG CAGCGAGCTC 1980
TGAAGGACGC TGCCTCCCTC CTGAAGTCGC AGACGTGGGC CCTGCAGCGA GCTCTGAAGG 2040
ACGCTGCCTC CCTCCTACTG AAGTCGCAGA CGTGGGCCCT 2080
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