Tag | Content |
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EnhancerAtlas ID | HS139-02776 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr1:110967580-110969130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr1:110969104-110969117 | ATTTAATTAATTT | - | 6.07 | Nkx2-5(var.2) | MA0503.1 | chr1:110968286-110968297 | CTTGAGTGCTT | - | 6.02 |
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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 |
GH01I110425 | chr1 | 110968501 | 110968650 |
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Enhancer Sequence | CTGTGTCTTT TTCATCTTTG CCCCTTTCCA CATGCTCTGG TTTGTAGAAC AGAATTGAAG 60 AAGGAGCCAT GTGCTAGATA GAGCGGGTTG GGAGCAGCAG ACCTGCCTGC TCATTGTTTC 120 TGTGACCTTG ACCCATCCTG TAGTCTCCCC ACGCCTTGCT ATTCTCATCC ATCAACGATG 180 AGATTGCACC TAAATCCTGG GTGCTGTGCT GGGCCTGGGG ATGCTGTCTA ATCCCTGGGT 240 TTCCTTCTAG TTTGCTCTAA TCACCCATAT GAAAAAGAAG CTACTCAAGG CAAACATATA 300 AATGAAACGG ATAATGAATG AATAGTATTT TTTCTTGCTT TCTTTGGAAG AGGCATCCTG 360 GATTCTACTT GAAGCCTGCA GCCCTGACTC CTGGGCTGGG AGGTGGGCGA GGACTTGTAT 420 TTTGTAGCTC TGCTAGAGAG GGAACAGCTG TCCACTGGTG GCAGGACTGA CGCCTCCCAG 480 AATACAGGGG CTTTGGATCA GCAGGCGTCA GAGGGAAAGG AAACTGGCAT CCGAGTCTGC 540 CTTTGAGAAA GGAGTAAATT ACTATCTTAT TATAAATTCA TGATCCACTC ATTGCTGTTT 600 TCAATTAATT TCTTGACAAA TCTGGCTGTT CCTTTTCTTA TTTTCCTTAG GACAGGAGGT 660 GTCCTGGTGA TCAGCTGGAG CTCGGGGGAG CTGTTGCTGA AATTAACTTG AGTGCTTTGG 720 AGAGAGATTT ACATGGCAGA GTGGAGCCAG GGCTGCTCCT TTGGCAGGCA CTGCTGTGCC 780 ACTGTGGAGG CGCCCCTGCT TTTCCCATGC TTTGCAGTGT CTTTAAAGGC CTTTGGAGCC 840 ATGCCCAGGC TCAGCCCCAT CCTGGTGTCC CCCTGTGTCC GTTTTGCCAC TGCCCGGCTA 900 CTTCACTTGG CCATGGGCCT TACCAGCTTG CAGACAAACC CGTCCATCTA CGCCTCCCAG 960 CGCAGCTTGG CCCACTTGCA AGCACTTACA GAGGGTTTCA GAAGGAACAT GTCTGCCATC 1020 TGTGTTTGGA GACTGTGTCC CAGACTTTTG AGCTCACATT AGTCATGGCC ACAGACGGGA 1080 CTGGAGTCCT GCCCACTGGA GTCCCAAAGG TCTCTGGTGT TTGTTTTCCA CTCTGCATGC 1140 CTGGGTTGGG GGATGGCAGG GGGATACAGG TTGTTGGAGT ACCTCCCAGC CGGGCCGTTT 1200 CCTTGGTTCC CTGGGGCTGC CTTGCTTCCT CTCTAGATCA TCAGTCTCAG CAGAGGAAAC 1260 CAAAAATCTC CTCCTCGCCC CGCAACCACC TTTTGCTGAC TGCTAAGCAT CCCTGCTCTG 1320 AAACCATAAC CACCATAAAA GCAATAGGCT TGTCTTCTCT GTTCTAAGCA TGTACTATTC 1380 AGGTGATTTA GGGGGAGTAA ACAGGCCCAG AGAAATTAAA TAATTTGTCT AAGGGTACCG 1440 GCTAATGAGG ATCTGAGCTC AGTTGTAAAT GACTCCATCA CCCATGCTCT TTTTTAGTCC 1500 CCTTTATAAT TATTTTAAAA TAACATTTAA TTAATTTTCT GTTATAAAAG 1550
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