Tag | Content |
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EnhancerAtlas ID | HS073-04910 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr16:517350-518460 |
Target genes | Number: 32 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EGR3 | MA0732.1 | chr16:517514-517529 | GGTGCGGGGGCGTCA | - | 6.15 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr16 | 518184 | 518382 | chr16 | 518038 | 518101 | chr16 | 518201 | 518385 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I000468 | chr16 | 518201 | 518400 |
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Enhancer Sequence | GACACTGAGC TGACTGCAGA GCTGACTGCA GAGTGGAGTG GGCGTCAGGG AGGAGGTGCA 60 GTAGCCTCAG GGAGGAGGTG CTGGGACGTC AGGGAGGAGG TGCAGGGGCC TCAGGGAGGA 120 GGTGCTGGGA CGTCAGGGAG GAGGTGCAGG GGCGTCAGGG AGGAGGTGCG GGGGCGTCAG 180 GGAGGAGGTG CAGGGGCCTC AGGGAGGAGG TGCTGGGACG TCAGGGAGGA GGTGCTGGGG 240 CCTCAGGGAG GAGGTGCTGG GGCGTCAGGG AGGAGGTGCT GGGGCCTCAG GGAGGAGGTG 300 CTGGGGCCTC AGGGAGGAGG TGCAGGGGCG TCAGGGAGGA GGTGCAGGGG CGTCAGGGAG 360 GAGGTGCTGG GGCCTCAGGG AGGAGGTGCA GGGGCCTCAG GGAGGAGGTG CAGGGGCGTC 420 AGGGAGGAGG TGCTGGGGCC TCAGGGAGGA GGTGCTGGGA CGTCAGGGAG GAGGTGCAGG 480 GGCCTCAGGG AGGAGGTGCT GGGGCCTCAG GGAGGAGGTG CTGGGACGTC AGGGAGGAGG 540 TGCAGGGGCC TCAGGGAGGA GGTGCAGGGG CGTCAGGGAG GAGGTGCAGG GGCGTCAGGG 600 AGGAGGTGCT GGGGCGTCAG GGAGGAGGTG CTGGGGCCTC AGGGAGGAGG TGCAGGGGCG 660 TTGGAGGAGG TGCAGGGAAG TCAGGGAGGA GGTGCAGGGG CGTTGGAGGA GGTGCAGGGA 720 AGTGAGGGAG GAGGTGCAGG GGCGTCAGGG AGGAGGTGCT GGGGCCTCAG GGAGGAGGTG 780 CAGGGGCCTC AGGGAGGAGG TGCAGGGGCC TCAGGGAGGA GGTGCAGGGG CGTCAGGGAG 840 GAGGTGCAGG GAAGTCAGGG AGGAGGTGCT GGGGCGTCAG GGAGGAGGTG CTGGGGCGTC 900 AGGGAGGAGG TGCAGGGAAG TCAGGGAGGA GGTGCAGGGG CGTCAGGGAG GAGGAGGTCC 960 TGGGGCGTCA GGGAGGCGGT GCTGCCATGG CATTGGACAC ATGGCCTCTG GGGCTGCGGG 1020 GTCTGCTTTA CTTTTGAGTA ATTTGATGTC ATGATTTATG TTTCGTTCGG AAGGAGAGTG 1080 AAACTAGAAT AAAACGAAGT CGAAGATGAT 1110
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