Tag | Content |
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EnhancerAtlas ID | HS098-13386 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:57751410-57753150 |
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) |
MEF2A | MA0052.3 | chr12:57751940-57751952 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr12:57751940-57751952 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr12:57751939-57751954 | TTCTATTTTTAGTAG | - | 6.57 | MEOX2 | MA0706.1 | chr12:57752563-57752573 | GTTAATTACT | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr12:57752918-57752933 | TGAACTCCTGACCTC | - | 6.22 | Zfx | MA0146.2 | chr12:57752013-57752027 | CCCGCCTAGGCCTC | + | 6.24 |
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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 |
GH12I057357 | chr12 | 57751585 | 57751906 |
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Enhancer Sequence | GCTTGTAGTT TTGCTGATTT TTTTTTTTTT TTTTTGGCTT TTTAGTTCAT TAATTTTTGC 60 TCTGGTCTTT ACAATTTCCT CTCCTTTGCT TACTTTTAGT TTGCTCTTCT TTTCTAATTT 120 CTTAAGGTCA ATGATTTTAG ATTTTTCTGC TTCCTAACTA TTTAATGCTA TAAACTTCCA 180 TTAAGCACTT CATTAATTGC ATCCCACAAA TTTTTCCATA TCATGTTCCC ATTTTCATTC 240 TGTTAACATT TTCTAATTTC CCTTATTAAT TCTTTGTTGA CAGAGTTTCA GAGTGGTTAG 300 GTTTCCAAAT ATTTGGGGAT TTTCCAGATA TTGTTATGTT ACTCATTTCT TTTTTTCTTT 360 TTTTTTTTTT AGACAGAGTT TCTCTCTGTC ACCCAGGCTG GAGTGTAGTG GCACGATCTC 420 GGATCATTTC AACCCCTGCC TCCCAGATTC AAGCAATTCT CCTGCCTCAG CTTCCCAAGT 480 AGCTGGGACT ACAGGCGCGT GACGCTACGC CCAGCTAATT TTTTTTTTTT TCTATTTTTA 540 GTAGATATGG GGTTTTGCCA TGCTGGCCAC GCTGGTCTTT AACTCCCAAT CTCAAGTGAT 600 CCGCCCGCCT AGGCCTCCCA AAGTGCTGGG GTTACAGGCG TGAGCCACCG CGCCCAGCCA 660 AATTTAGGAT TTAAATACAC AAAGTATGTT TTGTCATAAA GGGATTTAGT TAGAAATTAG 720 TAATAGAGGC CAAGTGGAGA AGTGTACGCC TGTAATCCTA GTACTTCGGG AGGTCAAGTT 780 GGGTGGATCA CTTGAGGCCA GGAGTTTGAC ACCAGGCTGG CCAATATGGC AAAACCCTGT 840 GTCCACCAAA AATACAAAAA AATAAAAAAA TTAGCTGGGC ATGGTACTGT GCACCTGTAC 900 CAACTACTTC AGAGGCTTAG GCAGGAGAAT CAGTTGAACC CAGAAGGTGG AGAGTGCAGT 960 GAGCCAAGAT GGCACCATTG CACTCCAGCC TGGGTGACAG AATGAGACTC CATCTCAAAA 1020 AAAAAAAAAA AAATTCTAAA TTTATTGAAA CTTATTTTAT GGCCCAAGAT ATGGTCTATT 1080 TTAGTAAACA TTCTATGAAT ACCAGTAAAG AATGTGTATC ATGCTGTTGT TGGAGTGGTT 1140 AAGTGTTAAC TGGGTTAATT ACTGATTTGT GTTTTACTTA TTCTACCAAT TATTTAGAGA 1200 GTGGTGTTGA AATCTCCAAC TATGCTATCC TCCCACCTCA GCACCCCGAG TAGCTGAGAC 1260 TACAGGCACA TGCCACCATG CCTGGCTAAA TTTTTTTCTT TTTTTTTTTT GAGGGAGTCT 1320 CGCTCTGTCA CCCAGACTGG AATGCAGTGG TGCAATCTCG GCTCACTGCA ACCTCCACCT 1380 CCTGGGTTCA AGTAATTCTC CTGCCTCAGC CTCCCGAGTA GCTGGGACTA CAGGCGCCCA 1440 TCACCACGCC CATCTAATTT TTGTATTTTT AGTAGAGGCG AGGTTTCACA TGTTGGCCAG 1500 GCTGGTCTTG AACTCCTGAC CTCAAATGAT CCAACCACCT CGGCCTCCCA AAGTGCCGGG 1560 ATTACAGGCG TGAACCACCG CGCCCAGTCC CCTGGCTAAT TTTTCTATTT TTTTGTAGAG 1620 ATGGTGTTTC GCCATGCTGC CCAAGCTGGT CTTGAACTCC TGAACCCAAG TGATCCACCT 1680 GTCTTTTCCT CCCAAAATGC TAGGTATAGG TATGCACCAC ACCTGCTTCA CATATTTGGA 1740
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