Tag | Content |
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EnhancerAtlas ID | HS184-08029 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:79960020-79961670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr12:79961527-79961537 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr12:79961527-79961537 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr12:79961527-79961537 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr12:79961527-79961537 | AACAGCTGTT | - | 6.02 | NEUROD2 | MA0668.1 | chr12:79961631-79961641 | ACCATATGGC | - | 6.02 |
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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 |
GH12I079565 | chr12 | 79959665 | 79961540 |
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Enhancer Sequence | GAAATTGTCC TGTGTGTATA ATTTCAAATT AATACATATA ATTGGACAAA TAAAATATCC 60 ACTTCCCAAT TAAAGTCTTT TTCTAGGTCA TAAAATAAAC CTTACTTTCA AACTTGTGCA 120 ATTCAGCAGA AAAAAATGTT TTGTTCTAGA CCCTTTCAAG TGCCCCGTGA CCTTCTCCCG 180 CAATGATTAA AAAAAAAAAA AACCCTATTG CCAACATCTA TACTTGCTGC CTTAAAGCAT 240 GCGTATGCAA ATCAATAAAA AATGCTTCTT GTTGTACAGG AACAGGAGCA GGTCAGTAGA 300 CAAGGAACTT CCTGCTTTGG TATGCTTCCT GTTTTCTGCT ATCAGGACAT ACCTGTAAGT 360 AGTAATCAGG ATCACTGAAA AAACAAATTG AGAAGTAGAG AAAAAAAATG ACTTGTTGCC 420 AACCCACGTG AATTCAAGCT AATTCATCCT GTTTATTTAG TTCCTGTTTC AGCTTGGTTA 480 ATGACACTTC CCTGGAATGT ATTTGTTTAG GAGTCCAAGC AGAGACATTT CTTACTAGGA 540 AAACAGGCCC AGGGTGAACC CAGAGATTTA GAGGAAAAGA AACCTAACGG GGAAATATTT 600 TAAGCTTCTC AAGTAAACTA ACTCAAGAAA CTTTCTTTCT AAAAGATGTT TTCCTTTACC 660 CAAGATTTTG TTCAATATTT CTTCAGTAGC TACAATTTAC CAGGGACTGT AGAGATTACA 720 TCTGTGTCAA TACATACTGC ATTCTTTTTT AGAACAGAGT TCTGATTTAC TTCAATTGGG 780 TTTCTAAGAG ACATAGAGTC TTCCTAGAAA AGCAGAAATT TATGACCAGA AGGCAGTTTT 840 GTTAATAGTC CAGAAGCTTC CTTATAACCT TTTTTTAAAA AAAGATTTTC AGGAAAGACA 900 ACCATTACAA TCTTCTCAAC TTCGCTACTG ATATAAACCA TATTATCCAT GAAAATGCAT 960 TGTTTCACAC AATTTACATG CATTATCTCA TTTGTTCTTC ACGATGACCC AACCAAGTTA 1020 GGCACTATTT TGTCCTTGCT GTAGAAGAGG AAACTGTAAA GCAACTTGCC CTACCTGACA 1080 GAGCTAGTAG TGGTAGAGCC AGGATTTGAA TTCAAGTAGG TCTAACTTGG AAGCTAGTGC 1140 TCAAGTGTGT CTGATTTGGA AGCTACCACT TCATTAGGTG GTGCTTGTAC AAACAGCCTT 1200 AAATACAGCA CTCAGGTGTA ATAACCATGG TTCAGTCAGA TGTTGAATGC ATTTTTCTAA 1260 ATATTTCTCT GATTGAAACC AATCTCTCCA TCTCAATTCC TTCAAAGCTT GCCTTAAATA 1320 CTAGATCCTA AAGAAGTCCC TCCTAGTCCT TTAAGGAACG AATTAATCTC TCTCCTTTGC 1380 TTGTGCACAT TCTGTTCTCT ATATGTAAGC TTTTTTGAGA ATGGAACCAG GCTGATTTCC 1440 TATGCACTCC TGGTGCTTCT CATACAGAAG TAAAAGGACC ATATCATACT TAAAGAAACA 1500 GGCCTCCAAC AGCTGTTTGT AATGCTGAAT TCAAATCATG TTCTAAAGAG GCAAGAATAA 1560 ATAAGCATTA ATTTCTACTC TGCTCAAAAA ATAGTTTTTA TAACTTCCTA TACCATATGG 1620 CTTGATAGTA TTTTGTAATC CCTAGTCTTT 1650
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