Tag | Content |
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EnhancerAtlas ID | HS116-24725 | Organism | Homo sapiens | Tissue/cell | Left_ventricle | Coordinate | chr3:134416130-134417620 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr3:134416266-134416278 | GGGCACGTGGCT | - | 6.18 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGAAGAGAT AAGCTTAGTG TTGGGTGGAG GCTTTGTCAT AACACTGTGG GATAAAACTT 60 GACAGGGTGT TTTCGATGGC AAGACATACA CACACTGCCC TCTCAAGCAG GGGCAGACCC 120 TCTGGCATTT AGTTTTGGGC ACGTGGCTTT CTGAAAACAT GCATGTAGAT GGGCTGTGTA 180 CAGGTCCTAC AACAGAATCC CACTTTAGAA AGAGGTATGG GGAGATGGAA GTGTTTGGAG 240 GACTACACCT TCCATGGCAT TCCTATGAGA CACAGTCTTC AAAGGTGCTG GAGTGTTCCC 300 AGCACTCATG CTCTTTGCTC GGCCCTCTTC CCTCATGATT GTACCCACAC CTGCACACAC 360 ACTGCTCACA GGCCTAAGCT AATGGGCCTC AGCTTATGGG CGGCAGATTT GCTTCTTTCA 420 GTAATGCCTG CTGATTCCCA CGTTCGTGTC AACTGTGTTG AGCTTTTGAG GCCTGTTCTT 480 ATCATTAGCA CTTAGCTTTT TCTTCTCATT TCCCAGTCAT TTTTGTAAAA TGACAAGAGT 540 AACCGACAGT AAACTATTCA ACCACTTGGG AAAATCAAGG AGTATGAAAC TGATGGGCTG 600 GGAGTGGAGC TCCAGCTGGC TGGCAGGCGG GGCCTGGAGC AGAATGTGGG TTGTCCTCTG 660 ATGCACACAT GTCCCTCCGT TAGGACACGA GTGTCAGATG CACAGCATGA ACATACAGGT 720 TGTCCAGACA TGGAAGACTG CGTGCACAGT CTTGCCATTC TGCTCAGGGT GTCTGATGGG 780 ATGGTGGAGA CATGGGCAGA TACCCCGCCA ACCTGACACC CCACGGCACA GCATGGATGG 840 CACACTTTCC AACTGCTTCA CCTTCAGCAG CTCTTATCAG TATTTGTTTT CAAACCAGCA 900 AGTTGTGTAT CCGTGCAGAG ATTCCCAAAG CAGCTAGGCT GCAGTGGAGA TCAGCTCTAG 960 GGCTTGGTAG GATAGCCAAA TATAGGTACC TGGACAGCTG ACTCTGGAAA GTTCTACAGA 1020 GCTGGCAAAG GGGCATGCCA AGCAGCACTT CAGTAGAGCC AGAGACCAAT AAATGGGATC 1080 TTTCATCAGA TAGGCTAGAT TCTCTGGCTT CTGAGTGAAG GGGGGCGGGA TGTGAGCAAA 1140 AGCAAAGGCT GCCAGTGAGG GCATGGAGGG GCTGCCGTCT CCATCCTCCA CCTCCAGGGC 1200 CAATTTCCAT AGAGATGGGA TTGGGAGGCC AGGAATGACC TGCCAAGAAT GCAGTCTCTT 1260 GCTGGAAGTT TGCAGCTGCT GCCTGTCAGG CAGAGATTAT TGAGAGGTGG CTCCAAACTG 1320 CTGCTAAAGC CTCACGCTCT GGAGAATAGG GTGCTGAGCT AACTCCAGGG TGGAGTGGGG 1380 AGCAGGTACA TGACCTCAGG CTGCCCTCGC CCACACCTTG TCTCCAGGTA GTCTGATACT 1440 GCTCTCTCCT TTCTCAGGCT ACCTCCATCA ATGTCTCCCA TGAAAAGACT 1490
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