Tag | Content |
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EnhancerAtlas ID | HS139-39791 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr3:195484200-195485990 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PAX5 | MA0014.3 | chr3:195484362-195484374 | CTGGTCACGCTC | - | 6.18 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGCCCCGGGG AAGATGAGAA TGTTGAGAGC TGGGAGACTC CTCGGCTCTG TGGTCTGATT 60 GCTGATACGG GGCTTCCCCC ACCCCTCTCA GGCCACCCTC CCCCTCCCCA GACAAATCTC 120 ATTGGTCATT TCCTTTGAGC AAGGCTGGTA TCGGGGGTGA TCCTGGTCAC GCTCCCAGCT 180 GGAAGGACGT GGCACCAGTC CAACATACTG ATTGTAGCGG GGAACGCCAC AGAGGGGAAA 240 GCAGTTTCCT CCTGAAGAAA CCCCAAAGGG CAGCCCTGGC TGGGCTCACA CCAGGATGGG 300 ACATCCTGGG GGATGGAGGA TCAAGGCCAG GATCCTCCAG ACACCTCCCC AGGCTGCGCT 360 GCCGGCCAAA CTGGCTTCAC TCTCACGGCA GCCCCATCCT TTGCCCTGAT TTCTCACCCA 420 CCCCCCACTT CCTGGACCTT TCCCAGACAC CCCCTTCAGA CACCAGACTG TAGTGAAACA 480 CTACTACATA TCTTCAGATC AAACTGATAT TTTTCAAGAA AATAGGAAAG TCTCCTTAAA 540 ACAGCAGATT GAAAGGAAGT GACAGAGAAT AGACGAACGT AATTTCCAGA CCATCGTCCT 600 TCAGGGGTGG GGCCCGTGGA GAAGAAAACC TCTCAGTGCC ATTGTCTCGC ACCTGGGAGG 660 ACGCACATGG GGCAAAAGGG ATGCAGGCAA AGCAGTCCCT TCTGAGACAC AGAGAGAAAG 720 AACATCAGGC AGAGAGGCAA AGAGAACGCA AAATATGCCC CCCGGGGCTT TGGTTTAGCC 780 AAGAACAGTC ACCCTCAGAA TTAGTGCTGG CAACAGACAG AAAGTGGCAT CCCTTTGATG 840 CCCTTGGACC CTTTGAATTA GTGCTGGCAA CAGACGAAAG CAGCGTCCCT TGTGCTTGGA 900 GCCTTTGGCC CTGATCATGG ATGTAGGGCT CGGGGTCTCT AACACCTTTA CGGAGAGGGA 960 GCGATGGCAC TCTACTGGGT CCTAGCCCAG GAAACCAGAC AAGGAGAGAC ACGGCTAGGT 1020 AAACATGGTT GCCAGACAAA AAGAGCAAGA AAGGTACCAA ACGAAAGTAT TTTTCATATT 1080 TCTTTAAATC TTGTCCTACA TTAGAGCCTT CCTTTAATAG ATATAAAAAT GTTGTAAATT 1140 GGTCATTTTA AATGTTGCAC TTGATTATTC TAATAATTTG GTGAATGCAT AATGACTAAA 1200 GATGACTATA TATGATCAGA TTGAGATTAA ATGATCTTCA AATCTTTTTT TTGAGACAGA 1260 GTCTCGCTCT GTCACCAGGC TGGAGTGCAG TGACGCGATC TCAGCTCACT GCAACATCTG 1320 CCTCCTGGGT TCAAGCGATT CTCCTGCCTC AGTCTCCTGA GTAGCTGGGA TTACAGGCAT 1380 GCACCACCAT GCCTGGCTTT TTTTTTTTTT TTTGTATTTT TAGTACAGAC GGGGTTTCAC 1440 CATGTTGGCC AGACTGGTCT CGAACTCCTG ACCTCAGATG ATCCGCCCAC CTCGGCCTCC 1500 CAAAGCGCTG GGATGACAGG CATGAGCCAC CGCGCCCAGC CTTGAATCAG TTCTATGTGC 1560 CCAGAGTCAC TCTAGCTATC TGGCCAAACC GCCGTAAGCC CGTCACTACT ACTTACTGGG 1620 GGGCACCTAT TTGAGTTATA GATATCGCTC CTCGGAAATG CCGGTCCTGG ATATTCAAAT 1680 GAAAGAGTGA CAGCAAGTGT TGCTGGGTGT AGCAATGCAG AATTTCCCAA ATTTGACTCT 1740 GACCTCATCC CCTACCCACC TCCCCACTCT CCCCAGCCAG CCAAATAGTC 1790
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