Tag | Content |
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EnhancerAtlas ID | HS060-14696 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr17:38104150-38105100 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr17:38104860-38104872 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr17:38104864-38104876 | AAACAAACAAAC | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 38104466 | 38104578 | chr17 | 38104811 | 38104910 |
| Enhancer Sequence | TCCGCCACCA GCTTCTTCCT GCCCTACAGA GCTGAGGCCT GGAGTGGCAG AGAAAGCCAA 60 GGGTACCCTG AGGGAGCACC CAGCTGAGGG GGAGTGAAGC TCCACCCCTT CCTGAATTGG 120 GCTCACAAAC AGAGGCTTCG AGAGCACAAC CCTAAGACTG AGGTCTCCTA CAGAGTGAGG 180 GGCATCAAAG CCAGAGGAAC CCGGGGAGCT TATTCCAAAG GGAGGGACTG CCTCCCCCAT 240 TGGACTAAAG GGAGTTCGAA CTGCTAGAAA TGGTTTCGCC TTAGCTCTCT GAGAATCTGC 300 CATCATCAAC CTCTCTTACC TCCAAGGAAC AGTCACCCCA AACCAGGAAG GCAAAGGGAA 360 AGCAGAACAA GGCCCCCAAG CTGCCAAATG GATGCCACCA CAAGCCCACC CCTTCATTCG 420 ACAAGAATCT GTTGGTCGGG CGCGGTGGCT CCAGCCAGTA ATCCCAGCAC TTTGGGAGAC 480 CAAGGTGGGC CCTGAGCTCA GGAGTTCGAG ACCAGCCTGG CCAAGATGGT GAAACCCCGT 540 CTCTACTAAA AATACAAAAA TTAGCCGGGT GTGGTGGTGC GGGCCTGTAA TCCTAGCTAC 600 TCAAGAGGCT GAGGCAGGAG GATCGCTTGA ACCCAGGAGG CAGAGGTTGC AGTGAGCCAA 660 GACCGTGCCA CTACACTCCA GCCTGGGTGA CAGAATGAGA CTCTGTCTCA AAACAAACAA 720 ACAAACACCA TCCGTTGAGT TCCTGTGCAT GGCAGGCGCT GCAACTACAA AGATCAGGAA 780 GTTGTGCCTG ACCCTGGGGA CCTGACAGGC TAGTGTATCA GTGATGACAG TCCAGGAAGA 840 CAGGGCTGTG CACAGGGGCC CTGTGAACCC ATAAGGAGCA TCTCAATCAA ACACCGACAA 900 AGGGTCATGT ACTTTGCTCA CAGGAACCCT CGCTCAGAAC TCATTTATTC 950
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