Tag | Content |
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EnhancerAtlas ID | HS184-00614 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:40605740-40607270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr1:40605788-40605799 | AACAGCTGCAG | + | 6.02 | Nr5a2 | MA0505.1 | chr1:40606862-40606877 | CCTGACCTTGAGCTG | - | 6.62 | Tcf12 | MA0521.1 | chr1:40605788-40605799 | AACAGCTGCAG | + | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 40605800 | 40606000 | chr1 | 40606000 | 40606476 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I040140 | chr1 | 40605873 | 40606190 | GH01I040141 | chr1 | 40606256 | 40606595 |
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Enhancer Sequence | AGTTTGCTAT GCCTGCTGTA ACAGTGTACC ACAAACTCGG TGGCTTAAAA CAGCTGCAGT 60 TCTCATGGTT CTGAAGTCCA GACATTCAAA ATCAACTTCA CTGGGCCCAA ATCAGGAATA 120 TTAACACGGC CATGCTTCCT CTGGGCTCTA GGGGAGAATT CGTTCCTTGC CTCTCCCAGC 180 TTCCAGCTGG CACTTGGCTT GTGGCTGCAC CACTCCAGTC TCTGCCTCCT GCCTTCTCCT 240 TTTGCGTAAT CTCTCTCTGC CTCTCTCTTA CAAGGATACT TGTGTTTGCA TTTAAAGTCC 300 ACTTGAATAA TCCAAGACAA TCTCCCCATC TCAAGTTCCT TGATCATATC TCTAAAGATC 360 CTTTTTCTGT ATATGATAAT ATTTACAGAT TCCAGAGATT AGAGCTTCAG GGGCCATTAC 420 TTAGCTTACT ACATCCTCAT TCTTTGAATA CTTCCTTTCT TCCTGAACCA GTAAGATTTT 480 TCACTGCCCT AGTCATGAAA TCAGCCATTT CTCTAAGAAC TTTTGGTTTC TTTTTAGTGA 540 AGAATGATAC TTGGAAGTCA AGATGTAGAT GCTAGGTGCA CTCATTGCTA TGGGTGTGTC 600 GGTCTTGCAA GTCCTTTCAG TAGGACAAGG AAACAAGATA TCAACTAGGA AAAATATGTC 660 TGGACACACA CACACACAAT CATACGTATG ATGTACATTC CGAAGTACTG TAGTGGAGTT 720 GGCTCATATG GACTTGCAAA AGCTGCTTGT TAAATATTCA GGAACTTTGC GGGTGGCTGT 780 GAAACTAGTA TTATTTCATG CTGGGAGTAT TTACACCGTG GAAATCAGCA AATGCTACAA 840 ATTAGTGTGT TTTGAAAAAC CAAAAAGCCA CTATACATAT CATAAACACA CACATCTACT 900 CTTCTGTCTC TCTTTGTATA TCATATATAA TATTCACACA CACACACACC CTATAGGCTC 960 ACACCTCTGA CTCTAATTAC AGGGTTTGTT CTAGTCTTTC CCCTTTTCAT ACTTATTGTC 1020 TCCAAGAGTA AGAAACCTGG CTCTCACTAT TCTCAATATA TTTTCTTATT TGCTCAATCT 1080 CCTGACCACA TGGGCCATCT CCTTGGCCCC ATTCTTACTG ACCCTGACCT TGAGCTGCAG 1140 GCTTTGCCAT GACCCTGCCA TTCCTGACCA TGAGAACCAT TTATTTGGCT CTGAACCTAG 1200 TTGTCCTGAC CTTGTAAGCT ACTACCTCAG CCCCAGACCT GCCAGCCCAG ATCACCAGAG 1260 TCTCCTTGGC CCAGGCTCCA CCAGCCCTAA ACTCACTTAA ACAACTCTTG GCCCCAGCCC 1320 TACACATTTT CTTGTTTGTC TATTCTTCCA ATTAAAAACG CCCACTTCGT CATTGTTTTT 1380 AACTGCCTGA TGTTGAGTGG TCAATTTGAT TTTTTCACAT GGTTGGGTTA AAGACAGGGT 1440 TGCCAGATAA AATACAGGAT GACCAGTTAA GTTGAATATG GGACATACAT ACTTATATTT 1500 AAAAATTATT TATTGTTTAT GTAACTCCAA 1530
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