Tag | Content |
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EnhancerAtlas ID | HS110-02860 | Organism | Homo sapiens | Tissue/cell | KATO3 | Coordinate | chr2:219176150-219177590 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SCRT1 | MA0743.1 | chr2:219176179-219176194 | GGGCAACAGGTGGGG | + | 6.03 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 219176294 | 219176891 | chr2 | 219176934 | 219177411 |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I218309 | chr2 | 219174616 | 219178319 |
| Enhancer Sequence | TTTACTATCT TAGCGAGGGG AGTGTAGCAG GGCAACAGGT GGGGAGAAGG TCAGCAGGGA 60 AACATGTGAG CAAAGGAATC TGTATCATGA ATAAGTTCAA GGAAAGGTAC TGTGCCTGGA 120 TGTGCACGTA GGCTAGATTT ATGTTTCTCT TTACCCAAAC ATCTCAGTGT AGCAAAGAGC 180 GACAGAGCAG TATTGCTGCC AGCATATCTC GCCTCCAGCC ATAGGACGGT TTTCTCCTAT 240 CTCAGAATAG AACAAATGGG AATGGTCAGC TTTACACCGA GACATTCCAT TCCCAGGGAA 300 GAGCAGGAGA CAGAAGCCTT CCTCTTATCT CAACTGCAAA GGGGCCTCCC TCTTTCACTA 360 CTCCTCAGCA CAGACCCTTT ATGGGTGTCA GGCCTTATGG TAAGGTCTTT CATTTCCCAT 420 GAGGCCATAT CTCAGGCTGT CTCAGTTGGG GGAAACCTTA GACAATACCC AAGCTTTCTT 480 GGGCAGAGGT CGGTCCCTGC GGCTTTCCGC AGTGCATTGT GTCCCTGGGT AATCGAGAAT 540 GGAGAATGGC GATGACTTTT ACCAAGCATA CTGCCTGCAA ACATATTGTT AACAAGGCAC 600 ATCCTGCACA GCCCTAAGTC CATTAAACTT TGATTCATTA CAGCACATGT TTCTGTGAGC 660 ACAGGGTTGG GGCTAAAGTT ACAGGTTAAC AGCGTCTCAA AGCAGAAACA ATTTTTCTTA 720 GTACAGATCA AAATGGAATT TCTTCTGTCT TCCTTTTCTA CATAGACACA GTAACAATCT 780 GATCTCTCTT TCTTTTCCCC ACATGTAAAG GCAAATATAA TTGCATTTGT TGTGAGAGCT 840 GAGGGTTAAT CTATGTAAAG CACTTAGAAC AGTGCCTTGC CTGTGATTTG TACTATATAA 900 ATATTTGCTA TTACTATCTG ATAGCAAGAA TTACATTACA TTCCTGGGTC TAACCAATAG 960 CTTGGCTGGC AATGTGTGGC TTGGACCAAG CAAGATCCAC CCATCAGGGC TGAGGAGGGA 1020 CTCACTTGAA GGCTATGGCT ATTCAGAGGA GAGTGGGCAA AATAGGGGTT AACAAGGAAA 1080 AAAGGGAGGG GTGAAGAATG GATATTGACC AACAGGATCT GCCACACCCA TGTTGTTTAA 1140 AAAAAAAAAA AAAAGAAAAC CTGGGCCGGG AGGGATGGCT CATGCCTGTA ATCCCAGCAC 1200 TCTGGGAGGC CAAGGTAGGT GGATCCCCTG AGCTCAGAAG TTCGAGACCA GCCTTGCCAA 1260 CATGGTGAAA TCCCATCCCT ACTAAAATTA CAAAAATTAG TTGGGTGTGG GGGTGTGCAC 1320 CTGTAGTCCC AGCTACTTGG GAGGCTGAGG CACAAGAATC TCTTGAACCC GGGAAGCAGA 1380 AGTTGTAGTG AGCCTAGAAC TTACCACTGC ACTCCAGCCC GGGTGACAGA GTGAGACTCC 1440
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