Tag | Content |
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EnhancerAtlas ID | HS064-11242 | Organism | Homo sapiens | Tissue/cell | GM18507 | Coordinate | chr4:3287550-3288540 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYB | MA0100.3 | chr4:3287875-3287885 | ACCAACTGTC | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 3287617 | 3288216 | chr4 | 3287595 | 3287800 |
| | Number: 1 | ID | Chromosome | Start | End |
GH04I003285 | chr4 | 3287075 | 3288537 |
| Enhancer Sequence | AGTTGTGCAT GGGCGGGACT CTGGGTTCTC ATGCCCTGGG GAGCGCCCGC GCCTGGGGCA 60 GGGCTCCGTA GACTCCTTTG TCACCCCTCA GCTTCGCCGT GAGGAAAATG TCCTGCAAAC 120 ACCAGCCCAG ATGGAGGGAG CCACGGCTTC ACCACTTCCT GCCGGTGTGC CGGGCTGCGC 180 TCCAGGGACC GCTGGGGCCG TCACCAAAAG AACGGAGCCC AGGGAACGTG GAGAGGAGCC 240 CAGATGCCTG AGGTGAGCAA GGCAGTGCCT CCGTCCAGCC TGGCATGTCC TTCTGGTTAT 300 TCGTGAGGCC ACCACAGGGA GGGTCACCAA CTGTCTGTTT TGCCTAGGAC CGAGGAGGTT 360 CCAGGGGTGC AGGACCTTTG ATGCTTAGAG CCAGGAGAGG CCACTCGGCC ACCCTAAGGG 420 CAGGTCTTCT GCCCCAGGCC GCGTGTGGTT TCTTTCGACA CACTGAGGAA GCCTTTCTCC 480 TGAGATCACC AAATGCAGCC TGCCCGGTTT CTGTTCCCCA TTACTGCGTA TGCGGTGGGC 540 AAACCTCCTC CGGCCCTGAA AGCTCCTGGC TGCCTGGGGA TTTTCTGTGT GCTCCTACAT 600 AAAAAGCAGC TTCTGTCACT CAACTGGCAA ATACAGTCTC AATTCAGAGT CAGTCCAAAT 660 CCATTACCCT AACCCTGAGA TATTAATCCA AGCTCCATTC TTGGTTTAAA GCCAGCCCCT 720 GTGGGCCCTG CTCCCCCGGC CTCCTGGGGT GGAAGCCTGT GCTGGGGGCT GCGGTGTGGG 780 GTTTGCTCTC CTCCCTCCCG CAGGTGGATG CAGGGCGAGG GAGTGAGGAG GAATGAGGGT 840 CAGGGGCAGG AAAGGCAGCC TGTGGCAGCC AGGCGGGGCC AGCGCTGCAC ACCGGGGAAA 900 GGCTCAGCGG GAACGTGTTC CCAGCACTTT GTCTCCCCAG GCCTCAGTTT CTGCATCTGT 960 AAACGGGCAT GTGCAGGGTT GTGAGAGGGT 990
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