Tag | Content |
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EnhancerAtlas ID | HS061-18518 | Organism | Homo sapiens | Tissue/cell | GM12892 | Coordinate | chr4:1741720-1742550 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr4:1742358-1742368 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr4:1742358-1742368 | AACAGCTGTT | - | 6.02 | MYC | MA0147.3 | chr4:1741749-1741761 | GGCCACGTGCCT | + | 6.07 | MYF6 | MA0667.1 | chr4:1742358-1742368 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr4:1742358-1742368 | AACAGCTGTT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGCCATGGG TGAGTGCCCG GGCCACCGAG GCCACGTGCC TCCACGAGGG GCTGCCTATG 60 CCCCACCCTG GCCCTGCCCT GCACCCTGCC TAGGACCCCA CCCTCCTGAG GCCCCTTTTC 120 CTAACACACG AGTCCCTTCA ACATGGGCCC GGCCGTGGAA GCACTGAGGC GAGTTGCGGG 180 GAAGCTGGTG GTAGTGAGGC TGGTGGCTCC CACGGAGCCA GGGCTTGGCA GGCCCCACAG 240 TTGTGCAGAT GCTGAGCTAG CAGTGGGGCT GTGGTGGGAG CAGAGTCTGT CCCGCCGTGG 300 CCTACCCCAC TCCACCCTGC CCTCGCCGTG CGGCTATGTC TAGCAGCAGC CTCTGTAGGT 360 GTCTGGCAGG ACGGGAACAC CAGGCCTCAT CTGGCCTCCC AAAAGCTTGG GCTCCTGGAG 420 GTGCTACTGT GGGGATCTGT CTTAGGCTGA GTGTCAGCCG GCGGCAGGTG ACCGCCTGGC 480 CCTTGCAGTC CCTCCAGGAC CACCACGAAG CACGACGCAC ATCCTGGAGC TCGCCATACC 540 GGCTCCCAGG CCTCACCCTA GGCTCTAGGG TGTTGGGCGC CGCCTCTTCA GGGACCTCTG 600 GCCCAGGCTC CAGTTCCCTG CGGATCTGAT GTGGAGGAAA CAGCTGTTTC CTGGGCTTTG 660 CATCCGGCCT AGAAGATCCT GGGTGGAGGG ACCCATCACC CTCCGAGGCT CACACCCACT 720 GCCCACCTCT CCTCCTGGCG CTCGAGTCCC TTGCCTCATT CCTTGGGCTG TCTCTGGCAC 780 CCATCGTTTC GGTTGCCTCC TCATCCTGAA CGTTTGCTTT TCTTTTCTCA 830
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