Tag | Content |
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EnhancerAtlas ID | HS178-01559 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr1:149992750-149994200 |
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) |
FOS | MA0476.1 | chr1:149993124-149993135 | AATGAGTCAGA | - | 6.32 | KLF4 | MA0039.3 | chr1:149992854-149992865 | ACAGGGTGTGG | - | 6.14 | MEF2C | MA0497.1 | chr1:149993440-149993455 | GAGCCAAAAATAGGA | + | 6.09 | Rxra | MA0512.2 | chr1:149993420-149993434 | AAGTTCAAGGGTCA | + | 6.07 | TBX21 | MA0690.1 | chr1:149993798-149993808 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr1:149993798-149993809 | AAGGTGTGAAT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr1 | 149993790 | 149993990 | chr1 | 149992800 | 149994200 | chr1 | 149993123 | 149993692 | chr1 | 149992763 | 149993068 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I150020 | chr1 | 149992536 | 149994920 |
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Enhancer Sequence | TAGGCCCCTA TCATATAATT ATCTGTGTCT GAAATCACAT TTCCCCCCAA AATGTTTGGT 60 GCACCTAAAT AACAACTGAC ACTTGTTGAT TGCTTAGTTT CCAAACAGGG TGTGGATCTT 120 TGACCCTAAC TTTATCTGGC CCTGTTCTGG TCTCTGCTGG GGCAGCGCCT TCCACCTTTT 180 CTCCTCTGGT TGGTTCAGTC TCCATCCCCT TACTTCTGTT GGCTAGACTT CTAATACGAC 240 AAAAGCAATT CATTTTTTGA GTACATAGTT TTAAATTTTT TCTGTTATTT TGAAGATTTT 300 TTTAATAGCA AATACATTGG CCCTTTTCTA TTTCTTTCTC TCAAAACACA CACACCCCTA 360 ACAATTGTTT TTAAAATGAG TCAGATTTTT CCCCCTTCGG GTCATATACT TCTAGTAGGA 420 AACATGTTCC ATTTTGCTAT ATCAGACAGT ATTTTGTTAA GGCTTTTGAC GTCTGTTTTT 480 TTCCAGTGGC GGTGAGGAAG AAGGTAGGCC AGGTCTGGGC AGGGTCCTAG AGGCTGGGAG 540 GACTGGAGTC AGGTTTTCAC ACACAGCAGC TGGGAGGGAA CAAAGCCAGA GGGTGAATGT 600 AAAACTATAT TTGGGGAGGT GTGGCAAAGG TTAATATTAA TCTGGAAAAA CGAGATCTTG 660 TCATCTTACC AAGTTCAAGG GTCAAATTCA GAGCCAAAAA TAGGAGATGA AGTCAGAGAT 720 CAGGAACTCA GTAAACCCAA GTCCAGTAGT TAAAGCAGAT ATGAGGTGAA AGGAACCAGT 780 GCTACAGAGT GAAACAGGTG GAGCCCCAGA GCTCCCTGTA TGGGATGAGT GAACCTGAAC 840 TAAGTCCGCA TTGGATTTAA TGAGAGAAGA CACGACAGCA CCAGCCCAGT GGAATCCAAG 900 TTCTAGTGCT CAGTGAATAC TTCTTGCATG ATAAAATGGG TTTACTAATT AGTCAACAAG 960 ATTTATGAAG CATATATAAG ATTCATTAAA ATGTGCATAT CACCAGCAAA TTTAGCAGCT 1020 TTCCTAAAGA GAGGCAGAAG GGAGAAAAAA GGTGTGAATG TTAACATTTA AAATTCATTA 1080 ACATTACAGA TGCAGTGGTT ACTCCAGACT TTCTCTTGCC ACTGAAACAA CATCTAATCC 1140 AGTCATTTAG AATACAGCTT CTTATTCCAA CATGAAGAAT AATCTAAACT CTCCCTTTCT 1200 CTCTCTCCTT AATCATTCTT CCTGCTTCCC AGCCTGAGCC TGGAACTTTT AATGGAAGTA 1260 ATGGGTCAAG TCAAGACTAG TTCCACAGTC TTTAGCTGTG TCAAATACTG TAAAATCTCA 1320 TGCTGGGCTG GGCATGGTGG CCCACACCAG TAATCCCAGC ACTTTGGAAG GCTGAGGCAG 1380 GTGGATCACC TGAGGTCGGG AGTTCGAGAC CAGCCTGGCC AACATGGTGA AACCCCGTCT 1440 CTACTAAAAA 1450
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