| Tag | Content |
|---|
EnhancerAtlas ID | HS047-06173 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr11:64682620-64684430 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr11:64683973-64683988 | GGGGTCAAGAGGTCA | + | 8.07 | | Nr2f6 | MA0677.1 | chr11:64683329-64683343 | AAGGTTAGAGGTCA | + | 6.06 | | RARA | MA0729.1 | chr11:64683973-64683991 | GGGGTCAAGAGGTCAGGG | + | 6.56 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 64682870 | 64682981 | | chr11 | 64682863 | 64683400 | | chr11 | 64683400 | 64683600 |
|
Enhancer Sequence | CCAACCCCAA ACACCTAGTG TAGCTGTGCC TCTCTGTGAG GCACAAGGCT GAGCCCCTGG 60
CTAAAATGTC CATGCTGGAG TTGTACCCCT GCCAACCTGG AAGCTCCTGG AGGGCTGTAC 120
CCCACCTGCC TCCCCCGTCA CCCCAGGTGC CACCCAGAAA GGGCCTCAGT AAACTGGTTG 180
GATCCAAGAA TAAAAAAGCA CATGGCAGAG CAGATGGGAG TCCAAATTCC TCACCCAGAG 240
ACCCACAGCT CGGGAAACTG AGGCCTAGAG ACAGGACTAA TCTAGTCACC CAGTATACAA 300
CAGGGACTGA GACTGGGATG CGGGCCTCTT TCTTTTCATG CCACTTCAGA GGCCCCAGAT 360
ACTCAGTTTC TTTGGGGGCC TTCAAGGCGG GGCCTGCAGG CTGAGCTGGG AGGGAGGAGG 420
GGCTGGTTAT CAAGAAAGCG CCTGCATTCC ACCAGGGCCC TAGAGAAGCC AATTCAATCC 480
CCAACAAGAG GGCAGGGAAC AGGAGTAGGG GCGTTTTCTG GAGCTGAAAG TAAAAAGGGG 540
AAGCCTAGGG CTGGGTATGG TGGTTCATGC CTATAATCTC AGCACTTTGG GAGGCTGAGG 600
TGGGAGGATC CCTTCAGGGG TTCAAGGCTA GCCTGGGCAA CATAGCGAAA TCCTGTCTCT 660
ATAAAAATAA AAAAGGGGCA GCCTAGAGAC GGCCTTAGAG GCTGAGGCTA AGGTTAGAGG 720
TCAGAGAGGG CTTCCTACAC CAGAATTCAC AGACAGCAGG CCACTGGGGG GTGCCCCCAG 780
TTCAGGGCCC ACGATTATCC TACCCCACAT TTGCTCACCA GGGCCTGGCC TACCCCCAAA 840
GCCTAGCTCT TCTGCCCAGA TTAGCAGCCC CCTGAGTCCA GCCACAAAAC TGAGAAGTCC 900
CTGCCTCCAT GCCCACCCCT GCTGCTCTGG ACCTGGTGGA TCGACCAGGA CGCGCCTCTA 960
ATTGGTGGCT CCTTCAAAGC TCCCCAGGTC AGCTGAGCTG TGAGTCAGGG CTCCTCACCG 1020
TTCCCAGCCT CAAGCCTCTG ACCTTACACC TCTTGGCCTC CCTAGCATCT CCCTTGGCCT 1080
CCTCCCGGCT TGAAGCCAGA TCTCCCCACC TTTCCTCCAG GGCCTCCCTC CAGGCAGGGA 1140
CACTGAGCCG GGGGGGTCGG TGGGAGATGT AGGTGGGGGC CATCCAGTCC CTCCCTAGAC 1200
ACCCACTTGG CCCATCCCAC TCTCCCAAAA GCAGGAAGTA GGCAGCGACC CAGGCACACG 1260
AGGTGTTGAT CAACACTGGT ACTGACGTAC TGACGCGGTT GTTGACATAC ACATCCGGTG 1320
GTTTGTTGAT CCCACCTACG GGCTCAGGAC CGTGGGGTCA AGAGGTCAGG GCACATGATC 1380
CACAGGTGTC CTCGCCAGGG CTCCGGACCC CTACCAGCTT CCCCCACCAG CTGCGCAGGC 1440
CCAAGTCTGT CACTGCCCTG GCCCAGCTCA GTTCCTACGC TCCCTCCCCA GCCCCTCCTC 1500
AGCCCGAGAG CCAACCTCCT TAACTCAGCC CCCAAACTCG ACGAGTTTGT CTTGCATTCT 1560
CCAGACAGGT GATCTTGCCC TCTCCAGCCT CAGTTTCTCC TCCCGTGGAG ACAGAAACCC 1620
CTTCCCGCTC AGTTTCTGGC TCTGGTAAGG AACTGAAGAG GCCAGCCGGG GTGCCTCTGA 1680
CGCCTGGAGA GGGCAAGATT CCCCTGGCCT CTCTACGCCC GGTGCCTGAT CCCCCAGCCC 1740
GATCCTGCCG CAGGGAGCCT CAGGTCGCTG CGCTCCCACC CTCCGCACCT TCCTGGACTC 1800
GGGCCTGGCT 1810
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