Tag | Content |
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EnhancerAtlas ID | HS139-37532 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr3:64563740-64565090 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:64563944-64563962 | TCTTCCTGCCTTCCTTTG | - | 6.36 | LMX1B | MA0703.2 | chr3:64565044-64565055 | AATTTAATTAA | + | 6.32 | PHOX2A | MA0713.1 | chr3:64565043-64565054 | TAATTTAATTA | + | 6.62 | PROP1 | MA0715.1 | chr3:64565043-64565054 | TAATTTAATTA | - | 6.32 | PROP1 | MA0715.1 | chr3:64565043-64565054 | TAATTTAATTA | + | 6.62 | Phox2b | MA0681.1 | chr3:64565043-64565054 | TAATTTAATTA | + | 6.62 |
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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 |
GH03I064578 | chr3 | 64563963 | 64564300 |
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Enhancer Sequence | GCCAACTCCA GAACTAAGAT TTGCATACGT GTCTGAGCCT GTATCCAGAG AAATGTATCT 60 CAGCAGCAGG GATAAAGGTC ATTTTAACCA TTATCAAATT AGATGCTCAT CCTCCAATTT 120 AGCATTGCTC TATCGGGAGG TTGGACAGCA CACAGTCACT CTCAATATGC ATTATTCAAG 180 TCCTTTGTGG CTTTTCTTGT CTCCTCTTCC TGCCTTCCTT TGGTTAAAAA AAAAAAAAGG 240 CTCAAAAGTA CCACTATGAA AGGACGGGAT GAGCAGTAAT AACCAGATAA AATGTAAATG 300 GCTCACAACA CAGAAGACTT GGCATTGAAA AAGGCTAAAA TTACATTTGA TGGTTTTCTG 360 CAAATTCAAA TGATTCCTAC ACTACTCTGA GATGTATTCA GATGGAAATC AAAAGATTGA 420 GGCAGAAGGG TGTAGTGGCT ATGAATACGG TGTTAGGACA GTCAGACCTG GTCTGACTGG 480 AAATATCTTT CTTTGTTATT TTTGGCAGGA TGCTTAACCA CTGCAAACAT CTATATTCAA 540 TTCTGTTTAA CAGAGATATG AAGTGATGAC GCCTACACAT CTCAAACTTA ACATGTTCAA 600 AACAGAAGTC CTGCTCTTCC TCCACAAATC TGTTCTTCCT GTAGGCTTCC CCATTTTAAT 660 CGGTGGCAAC TCCATCCTTT CACTTGTCCA GTCCATAAAA CGGGAGTCAT TGTGACCCCT 720 TTCTGACTCT TGCACCCCAT AGTCAACTCT CAGCTAATCC TTTGGCACTA TCTCAAAAAT 780 TCTTCCAAAT CCTACCACTC CTTACCACTT CCCTTGTGAC CACTGTCATC TGAGCAATGC 840 TTTCTCTCAT CTGAGTTACT ACAATGGTCT TACCACTTCC ATGTGTGTTC CTCCTGTACC 900 CTCTGCTAAA TCCAGAAGCC AGAGTCAACC TTTAAAAACA AATTCATGTT CCTGCTTAGT 960 GCCTCCACCC ACGTTTTCAC TGCCAGTCCC TTCCTATCTC AAAGTGAAAA CAAAAACTCC 1020 GTCCAATAGG CTAACCCTCC TTCCTCTACT TGCCCAACAG TCTGCCTCCA TGTTCGTCTC 1080 CCTCAGTTTC ATCTGTAATT TCCTATCCTA TCATTCACAT CCTCTGTTCT AGCCACATTA 1140 GTCTCTTTGG TATCACTAAG AGATGCCTGG TGTACTCCCG CTTTCAGGCC TTAACCTGTA 1200 ATACTCTTCT CCCAGATACT TACATGGCTT CCTTTTGTAT TTTCCCCTAT GTTTGCTCAA 1260 ATGTCACTTT CTTAATGGAG ACTTCCCTAA ACCTCCTTTT AATTAATTTA ATTAAGCTCT 1320 AATTTAATTT AATCTAATTC TCACCTACTC 1350
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