Tag | Content |
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EnhancerAtlas ID | HS067-02756 |
Organism | Homo sapiens |
Tissue/cell | GM18522 |
Coordinate | chr16:30609480-30610810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr16:30610578-30610590 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr16:30610599-30610611 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr16:30610603-30610615 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr16:30610607-30610619 | GTTTGTTTGTTT | + | 6.32 |
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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 |
GH16I030598 | chr16 | 30609322 | 30609922 |
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Enhancer Sequence | CTGGTCAAGG AAAACAATAC CTACAGTCAG ATCTGGAATT TGAGGCTGCC CTACTTATAG 60 GTTAATAAAT GGGTCTGTTA TTGTTTCATG GATGCTGTCA GAAAACAGAG ACAAAAGACC 120 TTACTGTTCA GGGCACAACA AGCAGCATGA GCATGCCTGC ATTGGTTCCC TTCTGCCCCC 180 TGCAGGGGCA ATGTGGGATG TGCCCAGATG GATGCTAGAC ACACAGTGAG TTGCATCATA 240 GGGGAGGAAC AGGAAGCTCC TGCTGTTTTT TTCCTTTTTA AAGATGGGAT TTGGCTGGGA 300 GCGGTGGCTC ACGCCTGTAA TCCCAGCACT TTGGGAGGCC AAGGCAGGCA GATCACCTGA 360 GGTCAGGAGT TCGAGACCAG CCTGACCAAC ATGGTGAAAC CCTGTCTCTA CAAAAATACT 420 AAAATTAGCT GGGCATGGTG GCAGGTGAGT GTAATCCCAG CTACTTGGGA GGCTGAGGCA 480 GGAAAGTTGC TTGAACCCAG GAGGTGGAGG TTGCAGTGAG CCAAGATCAC GCCACTGCAC 540 TCCAGCCTGG GTGACAAGAG TGAGACTCCT TCTCTAAATA AATACATAAA TAAATAAGAT 600 GGGGTCTTGC TATGTTGGCC AGGGTAGTCT CAAACTCCTG GCCTCAAGCA ATCCTCCTGC 660 CTTGGCCACC AAAAGTTCTG GGATTACAGT TGTGAGCCAC CATGCCCAGC CATCTGCTGT 720 TTTATAGTAA GCAGTAAGGA AGCTGCTCTT TGTCCTGGAT GCAGACATTA CCTCTCCCTC 780 AAGGTTTGCT TGCTGCCAAC ACTCCTGAGA ATTGTTCTGG GTAATGAGTG GCAAGGGCTT 840 TGCTTATTTA TTTTTATTTA TTGGTTATAC TTACATTTAT GGTTTATTAA AGCAAAACGA 900 CACAGATTTA AAATCATCAA AGGGATAAGG TACATGGGAC AAAATCCGGA TGCAACCGGG 960 CACAAACTTT CAGGTGTCTA CTCCCAGTGG GGTATCACAG GGACGTGCTT TTTTCTCCCT 1020 GCAATGATTT TTGACAACAG GTGCTGATTG TTCCCAAACA GAGAAGTTCA CCCAAGCTTT 1080 AGGGTGCAGG GTTTTTTTGT TTGTTTGTTT TGGTTTTTTG TTTGTTTGTT TGTTTGTTTA 1140 GATAGTCTTA CTTTTGTTGC CCAGGCTGGA GAGCAATGGT GCGATCTCAG CTTACTGCAA 1200 CCTCCACCTC CCAGGTTCAA GCAATTCTCC TGCCTCAGCC TCCCAAGTAG CTGGGATTAC 1260 AGGTGTGTGC CACCACCTGG CTAATTTTGT ATTTTTAGTA GAGACGGGGT TTCACCACGT 1320 TGGCCAGGCT 1330
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