Tag | Content |
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EnhancerAtlas ID | HS047-35635 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chrX:69653620-69654620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chrX:69653806-69653825 | TAGCTCCACCTTGTGGCCG | - | 7 | SP2 | MA0516.2 | chrX:69654309-69654326 | ACAAGACCCGCCCCCCA | + | 6.28 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI070433 | chrX | 69653051 | 69655901 |
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Enhancer Sequence | CATCTACGGT TGGATGGGAC ACGACCTTGA GGGGCCATCA GGGGGAGATG GGAGGAGGTG 60 GGTTGGAGGT GGGAGGAGAA TCACCTGCGG CAATGAAGGA CTCGCGGGAG GCTCGCGGGA 120 GGCCCGCAGG AGAGCAGCCA CCTCGGGGGC GTCCGGAGGC CGGGCGCGCG GTGCAGGGTT 180 GCACTGTAGC TCCACCTTGT GGCCGCCCCA AGAGGAGGGC CGCATCCGTC GTCGCCGTGA 240 CGTATTTGCT GAATGCCACC TGTTTTCCGT GCCGCTTGGG GACTCGTGTC CTTGACTCAG 300 GACTCCGAGG GCAAGGTCCG ATTTCCACAA GTTTTCGCTC CTCTGGGCTG CGCGCAGGGT 360 CCAATTTCCG GCCCAGCCTT CCCTTGGAGG AGCAAGTTCC CCAATGTGTT TGCGGCTCGG 420 GAGTCCCTGG GCTCCGCAGC TAAGGTGGCC AGTGCGGAGC TGACGGAGGA TGAAGAGTCT 480 AGTAGAAGAA GGGAGGGGCT AAGCCAAAAA TGGGGACAAG AGGGGCTCTG TGGTGACCCC 540 ACAGTCTTCC GCCACACCCA CATTCGACCT AGTTCGTATC TCCACACGGA GGGAAGTAGA 600 ACTAAGGAGT CGGCCAGGTA GGGAGGTCGG GTTCTCGGTT CCTCCTCTCT CGCCAGACTG 660 GGACCTGGGG CAGCACTGGC ATCCTCGGGA CAAGACCCGC CCCCCACCCT CGGTTGCCGG 720 GCAGCCGCGG GAACTACAAT TCCCAGTGAG TCCCCGGCCA TTTCCGGTAT CTGGCTGGAC 780 GCAGGCGAGT TTGAATCCGT GTTCCCGCCC CCTTCTCCCG GGCCCACCCC TTTCCTTTCT 840 GGCCGCCCCG CCCTCTCCGT GCGCATCCCT GCACACTCCG GCTCCGGAGG CCGGCCGCGC 900 CCACGTACCT GACCTGCAGC TGGCGCGGTG GGCGGGGGTG CCAGCATGCG ACGCACGGGG 960 AGGCTGGAGG CGCGCGGAGA GCGAACGCCG CAATCCGGTC 1000
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