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EnhancerAtlas ID | HS116-14999 | Organism | Homo sapiens | Tissue/cell | Left_ventricle | Coordinate | chr17:48804570-48805070 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr17:48804829-48804841 | GAATGTTTTTTT | + | 6.52 | HNF4G | MA0484.1 | chr17:48804888-48804903 | CGAGTTCAAAGGTCA | + | 6.52 | NR2C2 | MA0504.1 | chr17:48804888-48804903 | CGAGTTCAAAGGTCA | + | 6.55 | Nr2f6 | MA0677.1 | chr17:48804889-48804903 | GAGTTCAAAGGTCA | + | 7.19 | Rxra | MA0512.2 | chr17:48804889-48804903 | GAGTTCAAAGGTCA | + | 7.47 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTAGGGTCAG TAACTCTCTT AGTTGTTATA AAGGAATACC TGAGGTTGGA TAATTATAAA 60 GAAAAGAGGT TTATTTAGTT CAGTTCCCCA GACTGTACAA GAAGCATTGT AGCTGGTACC 120 TATCTGGTGA GGGTCCCAGA CTGCTTCCAC TCATGGCAGA AGGGGAGCTA GCATGCGCAA 180 AGATCACATG GCTAGAGTGC CAGGCTCTGT TCAACAACCA ATTTTCCAGT CAACTAAGAA 240 TGGGAATTCA CTCCCACAAG AATGTTTTTT TTGGGACCAA AGAAACCACA TCCAAACCAT 300 AGCAGTGCCC CAGCCCCCCG AGTTCAAAGG TCAGCTGTAT AGTGTACACA GGAAAGGAGT 360 GCATAACCCA GATTGGGATG GATACTCAGG AAAGGCCTGT CAGACAAAGT GGTCTTTAAA 420 TACATTTACC TAAAGGATTG GCAGGAATTA GCCTGAGGGA GAGGAGAGAG AAGACACCTT 480 ACCAGCCTGA AGGAAGAGCT 500
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