Tag | Content |
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EnhancerAtlas ID | HS073-05735 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr16:90018960-90020650 |
Target genes | Number: 22 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr16:90020391-90020403 | GGCCACGTGCCC | + | 7.22 |
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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 |
GH16I089953 | chr16 | 90019995 | 90020890 |
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Enhancer Sequence | TTCAGGAAGA AGGAGGAGTG ATGTTGGGAT GGCCTGATTT CTCCTGTGTC CTGGGTGCTC 60 CCTGGGAGAC TGGGGAGGTG CTGGCATCGG GTGGCCGCCT CTGACTCTGT GACCCACCCA 120 CAGTCATCAG GTAATAAGAG AAGGAGGTGG GACTGGGGCC CACTCACGTT CCCTGTGTCT 180 TCCCCGTGCC TCCCTGTTGG GGTCCACGGG CAGCCTGTCC ATGGGTGCTT TGTCCTTTCA 240 GGCTGGCGTG CAGGTGCCCA ACCCACACTC CTGCCCCACA GGCACAACAG GCAGGACAGG 300 CCCCATAGGT GGTGTGGAGT CTTGCCCAGT TGCAGGGCAG CCATGTGGGG TTGGGGTGGC 360 CTCCTTATCC CACTGCCAGT GAGGCAATTA GTTCAAATCC CAGTTCTTCC AGGCCACAGT 420 GTGACCCTGA GCAGGGCCGT CCCCTCTGGG CTCAGCTCTC TTTCTTTTGG GAGAAGAGAC 480 AGAGGATAAA TCATAGGATT GATTATTATA ATTGTGAATT ATTTCAGACT GTAGCAGGTG 540 TAGTGAAAGC ATAACTAACA CTGTAGCAGG TGTAGTGAAA GCATAACTAA CACTGTTGCA 600 GTTACTGAAC AACTTTAAAA AGACATCTCC GACTTTCTAT AACATCAACA GACCTTACAG 660 CGAGCTTACT TTGTGCTCAG TCTCTGTTAA CTCATTTCAC CCTCACAATG GCCCATTACG 720 GATGGGGAAA TGGAGGCAGA GAGGCTAAGG AATGTGGCCC AGGAAGTTAA GTGGGAGGGC 780 TGGATGCCAA CTGCCTCTAC TCCCACCCCA ACCAAAGTCC CTTCCTCCCT GCCAGGAGCC 840 ATCAGCCCTG TGTGTTCTGC AGTGTTCTGA GCCTCCGGGT GGGGAAAGAG CAATTCTTGA 900 TCCTGAGCTT CTGCCACGTG GAGAACTAGG CCCTTCCGGC CTGTTTCCTG GGTTCCTGAG 960 GCACAGAGCC GTGGGCCTGG TTCAGGTCGT GTTGCTCATC ACAGGATCAG AACCCAGGCC 1020 AGAGAGCCTG GATGCATTTG TAGGGGGCTT CTCTGTGTGC TGGCAGGGAA TCCTCCCAAG 1080 ATCCCCTGCT CCTGGGCATG GGGAAGGTGG GCCCTGCTCA CTCACCTGTG GCAGAGCAGG 1140 AATGGGCCCT GGAACTGTCC CCAAGTGTCC AACCCTAAGT CCTGAGACAG GGGCTGTGGT 1200 TTCAGGGTGC TCTGACAAGA AAGCACCTTT GCTTGGGGCC CAGGAAGGAG GAACCCATTT 1260 CTGAGAGGTG TGTCTCACAT AGCAGGTGGA TAGCAAGCTA GAGCGGGGCT GAGTGAGTAT 1320 CTGGGGCTGA GGCCCAGAGA GGATCCCATA GGTAGCTCTA GGGCTGGAGC TCTGCAACAT 1380 TGGGCAAGAG GACCCTGTGC TGGGAGGCAG GGAGCTTGGG CCCCTCAGAT GGGCCACGTG 1440 CCCTCGTGGG ACCCTCATTG TCACCGTGAG CTCTTTCCAA GGGGACGCCA CCAGTGGGGG 1500 CCTGGGCAGG AGGCAGCTGA GGTGTTTCAG GAAAAGGCTG AAGATCAAGG CTGTGGTGTG 1560 AGGACTACCC ACTTTAGGGA AGTGAAAGAG GCCAGCCTCA CCCCAGACAC CCCAGTGTGG 1620 TTGGGGAAAG GGGGTGGTCC GTGGTGAGCC TGGTACCTGG GGACTCATCC TGGCCCTGCC 1680 TGGCCCTCAG 1690
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