Tag | Content |
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EnhancerAtlas ID | HS043-18092 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr17:43116020-43117210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr17:43116217-43116227 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr17:43116217-43116227 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr17:43116217-43116227 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr17:43116217-43116227 | AACAGCTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_65506 | chr17:43115599-43116774 | Pancreatic_islets | SE_65506 | chr17:43116853-43117450 | Pancreatic_islets |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH17I045038 | chr17 | 43115721 | 43117197 |
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Enhancer Sequence | GGACAATGGC CAGAGCACAG ATGGAAATTC CAGCCTCCCG GGTTACCTAA TGAGTATCCT 60 CCCTTCTCAG TGCCTTGACC GAGTGTCTGT GGAAACAGAC CAACAGCTGC TTGGCCTCCA 120 TCAGGAAGGC CAAGCGGACA AAGGAGCACA CGCCCAGGGA GGCTCCGGGT CCCCAACTTA 180 AAAGGGCCTT GACAAATAAC AGCTGTTCCT GTCCAACAAG CCCCTCTGTA GCTCATTCCT 240 TCACTGACCA TCCACTGAGC ATCTCTGTGC TCTGCAGGAA CGGTGCCAGG GACCTCTTGG 300 GTAACCAGAG GAAAACACAA GTCTTGCCCC TTGGGAAAAC TGGAGAGCTA GATAGTACCA 360 GATGAAAACA TCTGAGAACA GAGCGCTGAC AGGTAAGCAG GAATGGTCAG GTGGTGCTGG 420 CCCTGGGCCT GCTGTATGAG TGCCTTCCCA CTCACTTGGC TGCGCACAGA TCTACTGGGA 480 TCTGCCAGGG AGGAAGTTGC AGCCCACGGT GCTCCCAAAG CTCAGCAAGG AGGAAATAGA 540 GGCTTAGGTA CCCAGCGGCC TCCAAGTCAC ACCTAGACCT GCCAGCAGCT CCCTGTCAGG 600 CCCACATGAA CAAACGACCA CCTTTGATCA CCTGTGTTCA TGACCCTCTT TCTGCTCTGG 660 TCAAGTCATC ATTCTCCAGA ATCCGATCTG GCTTCCCACA TTCCACTGCC GCTTACACAG 720 AGGCAGTACA TTCCTCACAG CAAGTGCTAA ACCTGGCTAT AATCTGAATT TACTGCGAAA 780 CTTACAAAAG GTACAGACAC CCAGGCTCCA TCTACCCCAG CCCACTGAAT CTGAATCAGC 840 TAGGCCCAGA ACCATGGCTA AAATGAAAGG CTGTGGACTG GAAGTGGAAA GTCCTGGGTC 900 CTGGTCTCTG AATTCTGTGA TAAAACTACC CATGTGACTG CAGGAAGTCT TCTCTCCAGC 960 CTGGCCCAGG GTGGTAAGGA CTCCATACAA GAAACAGCTG AGCCCCGGGT GCCTTCCCTC 1020 CTCTGAGCCT CAGTCCCCAC ACTTGTGAGT GAGAGGGGCT GGAGTTTCAG TGCCAAGAAC 1080 GGTGCAGCTC CCCAGGGAGG CTGAGAGTCA CACTGGTGAT TTCTTCCTCC CCTTCAGTGG 1140 TTCAGAGCTC TCCTGGGAGT GGTGAATAAA TGCTCCCCTG GGGCCAGGCG 1190
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