Tag | Content |
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EnhancerAtlas ID | HS098-48486 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:42928710-42929940 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr6:42928718-42928732 | CAGGCCGGGGCCGG | - | 6.78 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GGTGAGCCCA GGCCGGGGCC GGGGGCGTTG CATGAGATCG GGGTCTGTCT CAGCCTGTAC 60 TGCGCGGCCG CAGAACCACA GGGCCGGGCA CGTCAGGGCG GCCTTTGCCA ATCCTGGAAC 120 GGGTGGGACA CCAGGGCCAG GAGCAGGTAC CTGCCCGGCA GAACAGGCAC TGCGAGTGCC 180 CCGTGAGGCT AGGGGTCCAG GTAGCGGTTC GCAGGGAGAG GCCCCGGAGA AGGGAGACTG 240 AGTGTGAGTG AGGGTGTGGG CAGAAAAAGT GAGCGTCCCT GAGGCTTTGG AGCCAGAGCC 300 ACGGACAGAT TGCAAATATT CCTCCTGTGA TGGCCTTGGG CAGTGTTAAC AGTTAACATT 360 GCTCAACATT TGCACCTGCC AAGCCCAGTG CCAGGAGCTT TTGATACATC ACTTTTTCAA 420 ACCCTCACAA AGCCCCATGA AGTTAAGCAG TGATATTCTC TCATTTACTA CTGGGGAAGT 480 AAGGCCTCAG CAAAGTAAAA TTCCCTCATA CATCATCCAG TGAAAAGGAG CTAACAGGCC 540 CGGGTTGGTT AAGATCTGTC CTGTGCTCTA TTTTTCTCTT TTTTTTTTTT TTTTTTTTTG 600 AGATGAAGTC GTGCTCTGTC GCCCAGGCTG GAGTGCAGTG GCTCCATCTC GGCTCACTGC 660 AAGCTCCGCC TCCTGAGTTC ATGCCATTCT CCTGCCTCAG CCTCCCGAGT AGCTGGGACT 720 ACAGGCGCCT GCCACCACGC CCAGCTAATA TTTTGTATTT TTAGTAGAGA CGGGGTTTCG 780 CCGTGTTAGC CAGGATGGTC TCGATCTCCT GACCTTGTGA TCTGCCCACC TCGGCCTCCC 840 AAAGTGCTGG GATTACAGGC ATGAGCCACC GCGCCCGGCT TTGTCCTGTG CTCTAAACCA 900 CCATGTTCTA CTGCCTTTTG TGCACACGTA TTTTAACTTC AAGGAGCCTC AGCTTGTCTG 960 TCTCTCAAAT GGGAATGACA CTATTTACCT CTCAGGATTG CCATGAGAAT TAATGCATAT 1020 TTGTAGAGTG CCTGGCTCTG AAGAGGTGCT TTTAAAAAAA AGTTGCCTTG TGGTGACAGG 1080 AAACAGATTT GTGAGGTCAG TGGAGAGGGC CTGGGGAGAG GAGGCAGAGG AACGGACTCT 1140 GAGAAGTAGA GACAAAAGTG TCCAGTGCAG GGTCTCCTCC TGGCCCTCCC AGGCTCCCCT 1200 AACTGCCTCT CTCTGCCTCT CCTCGCTGGC 1230
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