Tag | Content |
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EnhancerAtlas ID | HS139-33632 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr20:56653700-56654770 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr20:56654358-56654370 | TGCCCCCAGACA | - | 6.44 | MAFF | MA0495.3 | chr20:56654156-56654171 | ATGCTTACTCAGCAA | + | 6.89 | MAFF | MA0495.3 | chr20:56654156-56654171 | ATGCTTACTCAGCAA | - | 7 | MAFK | MA0496.2 | chr20:56654154-56654173 | AGATGCTTACTCAGCAACC | - | 6.18 | RREB1 | MA0073.1 | chr20:56653731-56653751 | CCCCCACCCAACCATCACCA | + | 6.64 | SOX10 | MA0442.2 | chr20:56654202-56654213 | AAAACAAAGAC | + | 6.14 | Stat6 | MA0520.1 | chr20:56654130-56654145 | AGTTCACAGGAAATC | - | 6.01 | ZNF740 | MA0753.2 | chr20:56653722-56653735 | CTACCCCCCCCCC | + | 6.13 | ZNF740 | MA0753.2 | chr20:56653725-56653738 | CCCCCCCCCCCAC | + | 6.92 |
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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: 2 | ID | Chromosome | Start | End |
GH20I058078 | chr20 | 56653857 | 56654057 | GH20I058079 | chr20 | 56654061 | 56654230 |
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Enhancer Sequence | CCACCCCCCA CTCCTCCCTG CACTACCCCC CCCCCCACCC AACCATCACC ACCACCACCA 60 AGAGCAAACT CTAAGAGGAT CTCAGGTGTT TTCCTGGATC ACAGAAGCCC AGGGAGCAGA 120 CCCCACAGCT AACACTGACT CATGCCTCTT CCATGCCACC CCCTGCCCCT GTGCCCCAGA 180 GCCTCCCTTG GTTCATTTTT GGCAATCCTT GGTTCCTACA ATTCCTGCAG CTGCCTTGAT 240 TCAAACTCCC TCCCCAACTC CACCCCAGGC TTAAGGGTGG ACTGGATGGG AGCTGCAGGT 300 CATGGCGGAG GTCGGGGGGG ATCTCCAGCC AGTTACACCC CAAGGAGATG GAAATCAAAG 360 CCAATAGAAA CTCCTGTTGT TCACCAGCCC CTTCAAACAT CCTGCTTGGA GCAGATTCAG 420 GCTCTGGAAA AGTTCACAGG AAATCCTGGA GATCAGATGC TTACTCAGCA ACCACAAGCT 480 TTATCTTGGG TCTGAGTCCC AGAAAACAAA GACAAAAGTT TCTTCTAAGA CTCCCTTCTC 540 CCTTCGCCAA CTGGTGGAGC ACCATTTCCA AATAAAGGGG CTCCAAAAGC AATTCTAAAG 600 CAGAACTTGA AAGTCAAATC ACATTCTCAA AGCTCGTGCA GTTAAAACAC GGGTCAGATG 660 CCCCCAGACA GAGTCCCCCC ACAACCCGCC CTCCCACTAG CTGCAGAAAA GCAGCTAGGC 720 TTGAGCCGTT CAATTCAGTA GCCATTAGGA TTATGTGGTT CTTCAGCACC CAGTGTAGCC 780 AAGGAATTGA ATTTTTTAAG TTTAATAAAC TTAAACTTTA AAACTGAACA GTAACATATT 840 TGTCCATGAA GACAACTTTA TTGTTTTGTA GAACTACTTA CTGTATTCAT TTCCAATTGC 900 TACTGTGATG AATTACCAGA AACCTTGTCA CTTAAAACAA CAGGCTCGGT ACAGTGGCTC 960 AGGCCTGTAA TCCCAGCACT TCGGGAGGCT GTGGTGGGCG GATCACTTGA GTCCAGGAGT 1020 TCAAGACCCA ACTGAGCAAC ATGGTGAAAC CCCATCTCTA TTAAAATTAA 1070
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