Tag | Content |
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EnhancerAtlas ID | HS082-14260 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr17:5429320-5431670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr17:5430337-5430348 | AACAGCTGCAG | + | 6.02 | Tcf12 | MA0521.1 | chr17:5430337-5430348 | AACAGCTGCAG | + | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr17 | 5429332 | 5429441 | chr17 | 5430157 | 5430402 | chr17 | 5431009 | 5431369 | chr17 | 5429701 | 5430745 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I005525 | chr17 | 5428792 | 5431941 |
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Enhancer Sequence | AGTCTTGCTC TGTCACCCAG GCTGGAGTGC AGTGCACGAT CATGACTCAC TGTAGCCTTG 60 ACCTTCCAGG CTCAAGTGCT CCTCTCACCT CAGCCTCCTG AGTAGTTGGA ACTACAGGTG 120 CGCACCACCA TGCCTGGCTA ATTCTTCAAT ATTTTTTTGT GGAGATGGGG TCTCACTATG 180 TTGCCCAGGC TTGTCTCAGA CTCCTGGGCT CAAGTCATCC TCCCGTTTCT GCCTCCCAAA 240 GTGTTGGAAT TACAGGTGTG AGCCACTGCA CCCAGCCACT AAGGTATTTT GAATATCCAT 300 TTTGCTTAAT CTGAGTTTTG GGACTCTATA TTGTTATACG ATTCAGTAAG TGTTGGTTCC 360 AGGAAGACAA CAGTTTTGAG GCCTGAGGGA TACCACTGTG GTTTCCAGCC ATCTCATCTG 420 GTTGAACTCC TGAGTAGGTG GGCAGGGGGA GGGAGTGGGA ATGGGGCGAG ACCCCACTCA 480 GGTGTCTGTG TGAAGTGTTC TTGTTCCCAC AGGCAGCACA GAGAGGAGCA AGTGTGACAA 540 AAATGAGGGA ACTCACTTCC TCTTGGAGGG AGGGTTGTGT GGAGAGCAGA GGTCTGTGTG 600 TGCTGAAGGA GATGGGTGGG TGGGGGAACG AAGGACCCGA AGGACAAGGC CAGCTTCATG 660 GATGTGTGGC CTGTGCAGTC ACACAGGGTC CTGAGCTCAG CAGGGCTTGG TGCTTGGTTT 720 CATGTTTGGT GGTCTTGACA TTCTTAATCA TTTTTGAATG AAGAGCTCCG CGCTTTCATT 780 TTGTGCTGGG CCCTATGACT GCTGGAGCTG GTCCTGCAGG AGGGTGAGAA TGCCCATTGC 840 CACGGTGATG AAGCTGAGAG GCTGAAAGCC TCAAGCTCTA GCTATAGTGG GAGAAAACTC 900 ACCATGGAAA GTTAATGACT CATCACCCGT TCAGCGACGA CAGTGATGAA GCACCAGTGC 960 CCAAGTCCTA AATCAGACCC TGTGTCAGGC AGTGAGGTCA TCGTTTCCAG GGCAATGAAC 1020 AGCTGCAGCC CAGACAGCAG GCAGCAAGCA TTTCTGGAAG GGGCCCTGCC CGGCCCCAGG 1080 GATTGGTTTC CTGGCTGGTC ACAGCTAGCT AAAAGCAGCC TCTGTGCATT TTGCCTCTTG 1140 TTCTGTGGCA GGGGTGTCCA ATCTTTTGGC TTCCCTGGGT CACATTGGAA GAAGAAGAAT 1200 TGTCTTGGGC CACACATGTA AAATATACTA ACACTAATGA TAGCTGGTGA GCTTTAAAAA 1260 ATTCGCAAGA AAGTCTCATA ATGTTTTAAG AAAGTTTACG AATTCACGTT GGGCTTCATC 1320 GAAAGCCATC CTGGGCCGCA TGTGGCCCAC AGGCCGCAGG TTGTACAAGC TTGTGTACGG 1380 AGTCCAAAGG GAGTAAATCC TATCTGGCCA CAAGGTGAGG CTCAGAATTT GGTCTAGAGA 1440 AGGCTAGTGG GACATGGGCT TGGGCAGGAC TGGGGAGGGG TAGGGGTGTA GCTCTTAGCC 1500 TGGGATAAAC AGGACTTGGG ATAGAATCCC AACTCTGGAA GAGGGTCTTC ACCTCTCTCG 1560 GCTTCAGTTT CCTCACTGGT ACACCAAGGG AAAACTGTAG TGCCTAATTT CCCGGTTCAT 1620 TATGAAAAAA GAGATGATAT TAATATATAC GGAACTACCT TGCATGGTTC CAGGCACAGG 1680 ATGCTCAGTT ATTGTTCACA GTTCTTATTG GCCAAGTTCC AGTGCCACAA AGGACAGTGC 1740 CACAAGCACA GTGAATTCAT TCCTATTCTG ATTTGGCTGT CAGCCTGGCA GGCTTCAGCT 1800 AGATGCCTGT GCACTCGGAG GGTCACCCAA TTCCTTGGAC AAATCCCGTC TCCCAGGCCC 1860 ACTTGATGCA CGCAGGAGAC TGAGCAGGGC ATGGCCTGGG AGTCCTCACA ATGGGGAGGG 1920 CCAGCTCATC CACCTCTGAG AGTGGGGAAT GAGGGGGCGC TGGAGCAGGA CCTGAAGGCA 1980 GACTTTGTCC CCTCGGGCCC TGGTGGTACA TTCTGGCTCC AGACCTTAGC TGCATGAGGT 2040 TTCTCCTGGA ATACCCTGGT TAGAGCAGGG AGTGGTGGTG CAGCCCTGAG CATCCCAGGT 2100 TGGGGCAAGC CAAGTTCTTT TGCTGCTGGT CATGGGCAGA GCTACGACAG AGCTGAGCCC 2160 ACTGACTCTA TTAGCCAGGC CCCTCTCTTC TTGATAGAGT ACCTGGGGAT CCCTGGCCAC 2220 GGTCTCACTT GTGGAAGAGG CAGGCTGGTT GTGGTAGTGG CTGTGTTCAT TACTCTATAG 2280 ATTGCCCGGT GGGAACAAGT AACTTGTCCC AGCTTCTTGT TTCAGCCATC AGTTTCCTCT 2340 CCTCAATCTC 2350
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