Tag | Content |
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EnhancerAtlas ID | HS095-12794 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr17:46013040-46013890 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr17:46013101-46013113 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr17:46013105-46013117 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr17:46013109-46013121 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr17:46013113-46013125 | AAACAAACAAAC | - | 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I047935 | chr17 | 46013021 | 46014114 |
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Enhancer Sequence | GTGAGCTATG AGTGTGCCAC CGTATTCCAG CCTGGGCAAC AGAGTAAGAC CCTGTCTCAA 60 AAAACAAACA AACAAACAAA CAAACAAAAA AAACGAAAGA AAAGAAAAAA AACCAAAACA 120 ACAAAACACA CACTCAGCCC TGCTCCCACC ATGTGCAAAA ATGTCCTGCA CCCTACTCAC 180 CATACGTAAC ACCCATCATA CTGAAAAGCT TAAAAAAGTG GTTTATGCAT AAACATTACA 240 GATTAGCATT TTTTGAGCAC ACCTTGTGGG CTAGGATTGT GAGAAGAAGC CAGAGAAAGT 300 TAAGAGATGT GGTCCCTCTC GTGAAGGAGG TCCCATTCTA ACAGGGAATA CCAGCCACCC 360 ACAATGTATT TGGGAAGCCA TCTATAAGCA CATGCAAGGA TCGTTTAGAG GGTTAGCCAC 420 AAGCACCAAC AGGCAGGACA CCGATAAGTT TCAGCCTCCT CTGATCTCGT CCCAAGCCTC 480 TGAGGACCCA CCTCCCTTGG GCCTCTGATA AACCCACTCA GGGCTTAGGC ATCTGCTGGC 540 AGAGCACCAA GCACACGCCC TTCTGTAAGT CCTGGTGTTG CTACTCTTGG GGCTCCAAGC 600 TGAGTTCACT TCAAGGCTGG GCCCAAGAAT TCCTGAGCTT CAGGCCCTCC AGCACACCCC 660 TTGCTCTGCT ATCAGCCTTC TTCCTCTCAC CTCTTAGAAA GCTGGACACA GGCCGGGCAT 720 GGTGGCACAC ACCTGTAATC CCAGCACTTT GGGAGGCTGA GGCAGGCGGA TCACCTGAGG 780 TCAGGAGTTT GAGACCAGCC TGGCCAACAT GGTGAAACCC CGTCTCTACT AAAAATACAA 840 AAATTATCCG 850
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