Tag | Content |
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EnhancerAtlas ID | HS139-39920 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr4:1683900-1685420 |
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) |
MEF2A | MA0052.3 | chr4:1684160-1684172 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr4:1684160-1684172 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr4:1684159-1684174 | TTCTATTTTTAGTAG | - | 6.57 | NKX2-3 | MA0672.1 | chr4:1684558-1684568 | TTCAAGTGGT | - | 6.02 | Zfx | MA0146.2 | chr4:1684231-1684245 | CCCGCCTCGGCCTC | + | 6.01 |
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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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Enhancer Sequence | AACAAATGCT TAACAGATTG TGAAATTCAA TTTTTCTTTA ATATCATTGC AGAAAATGCC 60 AAAAGAGTTT ATATAAAAAT TTTTAATTTC CTTTTTTTTT TTTTTTTTGA GACAGAGTCT 120 GGCTCTGTCA TCACGGTGGC GTGCAGTGGC GCCATCTTGG CTCACTGCAA CCTCCGCCTC 180 CTGGGTTCAA ATGATTCTCC TGCCTCAGCC TCCCGAGTAG CTGGGATTAC AGGCACGCAC 240 CACCACACCC AGTTAATTTT TCTATTTTTA GTAGAGACGG GGTTTCACCA TGTTGGCCAG 300 GATGGTCTCG ATCTCCTGAC CTCGTGATCT GCCCGCCTCG GCCTCTCAAA GTGCTGGGAT 360 TACAGGTGTG AGCCACCGCG CCTAGCCTTA ATTTCCTTTT TTAGAAAAAC ATTTTCCCTG 420 TTCCCAATGC ACCGGTGAAA AATACCTGTT TTCTTAGTTC TTTTATCTAC CAGCTAAAAA 480 TGTGTACTCT CTCGGATTAG AGCCTCTTCC TATTTCTGTT TCCTGTGCAC ATCATTGCAT 540 GTGAGCAACT ACCTCTATAA CTAGAAAGGC CTCACTATAG AGCAACTACC TCTATAACTA 600 GAAATGCATG CACTAAAAAA AAAAAGAAAA AATTACTTTG GCATTTTCTC TTATATACTT 660 CAAGTGGTAA CAAAAACGTT CTGTGGTCCC CACGTGCAAT CTAAGAAACA TAAGGACGCA 720 TCCAAAGGGG CGGGACAATT ACCAAGGCCT CAGTGAGTGT GACCCTCAAA GTCGCAACAC 780 AGAACACAAC AGAGGGACAA AGCTGCAGAA TCAAAAGCTC TAAGTTCACG GGACAGCACG 840 GGGAATCAAC TATCAAGCCA CAGAAGGGGA TCAGGACTGC CAGTACCCAG CGCACAAGGA 900 GGACTCAAGG AGGCGGGACA ATGGCGCCGG ACGAGGGAAA ACTACAATTG TCTGAAAGAA 960 CTACCACCTA GTTTTCCTGC GCTAACTAAC CCAATTTAAA GAAAAGTCAC TGTTTCTAAA 1020 CAATGTCAGT TTCCATTTTG GGGTAATATT GAAGAGCTTC AAATAAATCA AAACCGTTTC 1080 CCAGCCTACC TTCAGGGTGC AAGGGTGCAC TTCCCTTCTA GCACCCACTC TGATGAGGGA 1140 GAAGGTCAGG CGACAGGAGG GTGTTTAAAG CAGCATCAAT ATGTTCAGGT TAAATTTCTT 1200 AAATATTGTG AAACGGAAGC ACATTCTTTT CCTTTTCTGT TTCGTTTTAA GACTAGTCAA 1260 GTGCAGTAGT GAGAAAGGGG AAAGAGTGGA ACAAGGAGTT CGATCTGTAA TGGACTGAAC 1320 AAGCAACAGA GAAAACTCAC TCCCTTGGCA CCAGCCACGA GCACATTCTT GAAGCCAAAC 1380 TCATCCATCC GTACTGGGAG ATAGATGATC ATAGAAACAT CAAGTGTGAG TCTGGTTTGA 1440 GTTTAAAACG AAAAGTGCTT TAGAGTTATG GAAACTTAGC TTCAAAGAAG AGGCACCAAG 1500 GATGCCGCGC GAAAACTCAC 1520
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