Tag | Content |
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EnhancerAtlas ID | HS183-03891 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr3:195484190-195485990 | 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 | TCCCATTCTC TGCCCCGGGG AAGATGAGAA TGTTGAGAGC TGGGAGACTC CTCGGCTCTG 60 TGGTCTGATT GCTGATACGG GGCTTCCCCC ACCCCTCTCA GGCCACCCTC CCCCTCCCCA 120 GACAAATCTC ATTGGTCATT TCCTTTGAGC AAGGCTGGTA TCGGGGGTGA TCCTGGTCAC 180 GCTCCCAGCT GGAAGGACGT GGCACCAGTC CAACATACTG ATTGTAGCGG GGAACGCCAC 240 AGAGGGGAAA GCAGTTTCCT CCTGAAGAAA CCCCAAAGGG CAGCCCTGGC TGGGCTCACA 300 CCAGGATGGG ACATCCTGGG GGATGGAGGA TCAAGGCCAG GATCCTCCAG ACACCTCCCC 360 AGGCTGCGCT GCCGGCCAAA CTGGCTTCAC TCTCACGGCA GCCCCATCCT TTGCCCTGAT 420 TTCTCACCCA CCCCCCACTT CCTGGACCTT TCCCAGACAC CCCCTTCAGA CACCAGACTG 480 TAGTGAAACA CTACTACATA TCTTCAGATC AAACTGATAT TTTTCAAGAA AATAGGAAAG 540 TCTCCTTAAA ACAGCAGATT GAAAGGAAGT GACAGAGAAT AGACGAACGT AATTTCCAGA 600 CCATCGTCCT TCAGGGGTGG GGCCCGTGGA GAAGAAAACC TCTCAGTGCC ATTGTCTCGC 660 ACCTGGGAGG ACGCACATGG GGCAAAAGGG ATGCAGGCAA AGCAGTCCCT TCTGAGACAC 720 AGAGAGAAAG AACATCAGGC AGAGAGGCAA AGAGAACGCA AAATATGCCC CCCGGGGCTT 780 TGGTTTAGCC AAGAACAGTC ACCCTCAGAA TTAGTGCTGG CAACAGACAG AAAGTGGCAT 840 CCCTTTGATG CCCTTGGACC CTTTGAATTA GTGCTGGCAA CAGACGAAAG CAGCGTCCCT 900 TGTGCTTGGA GCCTTTGGCC CTGATCATGG ATGTAGGGCT CGGGGTCTCT AACACCTTTA 960 CGGAGAGGGA GCGATGGCAC TCTACTGGGT CCTAGCCCAG GAAACCAGAC AAGGAGAGAC 1020 ACGGCTAGGT AAACATGGTT GCCAGACAAA AAGAGCAAGA AAGGTACCAA ACGAAAGTAT 1080 TTTTCATATT TCTTTAAATC TTGTCCTACA TTAGAGCCTT CCTTTAATAG ATATAAAAAT 1140 GTTGTAAATT GGTCATTTTA AATGTTGCAC TTGATTATTC TAATAATTTG GTGAATGCAT 1200 AATGACTAAA GATGACTATA TATGATCAGA TTGAGATTAA ATGATCTTCA AATCTTTTTT 1260 TTGAGACAGA GTCTCGCTCT GTCACCAGGC TGGAGTGCAG TGACGCGATC TCAGCTCACT 1320 GCAACATCTG CCTCCTGGGT TCAAGCGATT CTCCTGCCTC AGTCTCCTGA GTAGCTGGGA 1380 TTACAGGCAT GCACCACCAT GCCTGGCTTT TTTTTTTTTT TTTGTATTTT TAGTACAGAC 1440 GGGGTTTCAC CATGTTGGCC AGACTGGTCT CGAACTCCTG ACCTCAGATG ATCCGCCCAC 1500 CTCGGCCTCC CAAAGCGCTG GGATGACAGG CATGAGCCAC CGCGCCCAGC CTTGAATCAG 1560 TTCTATGTGC CCAGAGTCAC TCTAGCTATC TGGCCAAACC GCCGTAAGCC CGTCACTACT 1620 ACTTACTGGG GGGCACCTAT TTGAGTTATA GATATCGCTC CTCGGAAATG CCGGTCCTGG 1680 ATATTCAAAT GAAAGAGTGA CAGCAAGTGT TGCTGGGTGT AGCAATGCAG AATTTCCCAA 1740 ATTTGACTCT GACCTCATCC CCTACCCACC TCCCCACTCT CCCCAGCCAG CCAAATAGTC 1800
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