Tag | Content |
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EnhancerAtlas ID | HS139-29478 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr2:95999350-96000970 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RELA | MA0107.1 | chr2:95999761-95999771 | GGAAATTCCC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 95999501 | 96000056 | chr2 | 96000725 | 96000969 |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I095333 | chr2 | 95998773 | 96002010 |
| Enhancer Sequence | GTAGCCTCTG TTGGTTGCAA TTGTGACAGC TCGTAGGAGC ATGGTGAGGA TTCAATGATA 60 CTATGTCAGT GAGTGCCTAG GACAGTGCCT GGCACATGGT AAGCAGCAAT GAATGACACT 120 GCTGCTATCC ATTATTATTA CCCAATTCCC TCACTGAACG CAGAGGGCAT GATGGGTGGC 180 TGAGTCCTCC CAGCTTCCTT GAGGCAAAGG TGGGACTTGG ATAGGGGGCG TCTCACTCCT 240 GCCCAGCACC CTGGCTGCTC CCCTGCTGCT TTCTGACTCA GACCCCAAGG TTGTGATTCC 300 CAAGTCATTC GTCTGCATTC AGCTGACACA GGCCATCTGC AAGACACACA CCTCTCTGAG 360 CTGTCAGAAG ACACTGCAGA AGCTGAGATC CTGGCATCAA GCGTCCCAGA TGGAAATTCC 420 CCAAGACACC CTTGGGCCCT CGGCTCAAGT TCAAACAAAG AAATGCTTAT GTTCAGAGAT 480 CTTCACAGAT CACCAGCGAG GATGTGACTT GAGAACACTT TGCGTCAGCA TCATAAAACA 540 TGAGGATTGA TGACCCGTGT GAGTGGGGCG AGTGCCAGGG GAACACAGGC TCTGAGTTGG 600 CCGGCCGTGC TTCCTGCATA CACTCTGTGC AGAGGGTGCC AGCCTAGACT GGCGGGGGGG 660 TTAGAATAGC ACCGCACTAG TTAGCATGTC CCATAGGACC CTGTTTACAG CACACTTGCA 720 TGGGCATGTG TGCACCTGGT TCTCATGACA ATATGCAGGG TGGGCAGGGG TTAAGGAATG 780 CTTCCCCACT TTGGGGATGA AGGAAACTGA GGCTCAAGGA GGTGCGAAGC CAGGCAGCTG 840 AGGTCACACA GCCTTGGATC TCCCTACCGT CACTATCCTC CCCTCTTGCC AGCAGAGAGA 900 GGTGGGAAAG CCACGTTCAG CCAAAACCCA GAAATTTACC CAGAGAAACT CACAAACCAA 960 CATGGTGGGC CTTGTACAAA CTCTAAGAGT ATGAAGAGAA GAGCTACAGC TGGCCTTACC 1020 CAGTCCTGCC ATGCTGGGAC TGGTCAGCTC CCCTGCACTG AATCTGGGTA GGGGCATGAA 1080 AAGACACAAG ATGGGATGAG AAATCCTCCA CATGGGAGAG GAAATGGGAA CCTTTCATCA 1140 CTGGGGACCA GGAAGCAGGG TGAGGGGCTC ACAGGACAAG CTGGCCTCAA ACGTTCCCCT 1200 TCCATTGCCT GTTCAATGTT ACTAGATACT TGCAGACCTC TGGCAGAACA GATGGGGACT 1260 TGGATATACC TTGTAAGGGG ATGGGGGCAT GAAGACAGAT TCGTTCCCCT GACCAAGGGG 1320 GAATCAAACA GGTCACTGAG CGCTCAAAGG AGAATATTCC CAGAGCTATG CAGTGAGGGG 1380 CCTGCTACCA CAGTAACACT TGGGCATGTG TCAAGTCCCC ACTTGGCCAA GTAGCTTGGT 1440 CTTCTCCTAC CTTCCAAGTC TTTCCTGACC ATGAGAACCA TGGGAACCAG AACTACTTAA 1500 TTAAGAACAT GAAATTCCTT TCCTTTCAGA TCACTGGTCC TGACTCTGGC CTGAGATGCT 1560 AAGAGATCCC ACAGCTCCTG TGATGGGAAA AGATCTATTC CCAGAATGTG GTTCCCACAT 1620
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