Tag | Content |
---|
EnhancerAtlas ID | HS128-03531 | Organism | Homo sapiens | Tissue/cell | MCF-7 | Coordinate | chr11:13050970-13053560 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr11:13052270-13052280 | ACCACTTGAG | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH11I013030 | chr11 | 13052481 | 13052630 |
| Enhancer Sequence | AGACATGTAC GAGCTGTTTA GGAGCTAGCC TCATTCACAT GTCATGATGA ATCATTGGTA 60 TAGGGTGAGA GAGGAGTAGC CTAGAATGAA TCTCAGTATT CCAGCTTGGG CATAGGGAAA 120 GATACGGGTG GGGGCTCCTT AGATGGTGTG GAATAGGTCT TGGCCAGCAG TGGGGGTAAG 180 AGGTGGTGAA GTTACTTTGG AAGATATTGA GTTGAGGTGT GTGTGTGTGG ATATTATCTG 240 AAGACAGGAC GGGGCAGCCA TGGACAGGGA TTTAGCTGCT CAAAGAAATG TGTAGAGTGG 300 GAAGGGAAGA AGACTGAAGA TGGGGCTCTG GAGAAGACTG ATATTTAAAC AGTAGATAAA 360 AGGAGAGGAA TACACAAAGA CTAAGAAAGA ACAGAGAAGT AGGAAAAGAA GGAAAAGGTA 420 ACATTGTGAA AATGACCTTT GAGGGAGTGA GTTTCAAGAC TAGATGGCCA CCTGACCTCA 480 TCAGGTTTGG CAATGTATAA ATATAACCTT GAAAAGAGTA GTGCGAGTAG ATTGGTGGAA 540 ACCAAAGCCA CATTCAGTGG CTTGAGGAGC AAGTGGGAAG TGGGAAGTTG GAGACAGCAA 600 GGAATAAGAA CTCATTTGAG AGGTTTGGTA TGATGGGGTA AAGATACGAC TGTAGTTGTA 660 AAAGGATGAA GGTCCAAGGA AGAATGGCAG ACAAGGGGGA GGGAGATCCG AGATGAGGCT 720 GAAGAAGTAG GTGGGAGGCA CAACATGCAG AGCCCAGGAG GCCACAGGAA GGAGTTTGGA 780 TTGTATTTGC AATGTCCTGA TTATCAGGGA ACAGATTTAA GCAGGTGAAT GATGTGACCT 840 GACCCCTCTG GCTGCTCAGT CAATGACAGA GGAAGGGAAC AACCAGGGTT TGACTTTCTC 900 AAGGTGGAGA CGGTCCATAA TGAGGCCCTG GCAGTGGGTG GCTGAAGAGG TCTGCTGAAG 960 GTGAGGGTCA CCGAAGCCAG AAGCCAAAGC TGTTAGGAGA CCCAAAGGAC CCACGGTGAT 1020 GCCAGGAATT GGAATGGAGA GAGGAAAAGG TCTGGGGTGA GGGAACAGCG GGAGGTCAGT 1080 CAATGGAAGC AGGGTCGTGA CTCGGGAAGG TTTGCACTGG GGCAGTGGCT AAGGACAAGG 1140 GGACAAATGA CCCTGTAACT CTGAGCATGT TCCTCCTCTG TTCAGCATTC ATCAAAACTC 1200 TCTATTACCC ACTGGAGAAT GCCCAAACAT CTCAGCCCTG TCCTGCACAA TACATCTTAA 1260 CAGCCTCATC TCCCACTCCA CTCTCCCCCA GACCCATTGA ACCACTTGAG GTTTCCTGAA 1320 CATGCTATGC TGTCCATACC ACTCTCCGTT TGCACACAGC ACTCCTCCCA TCTGAAATAT 1380 CTGTCTCTTC TTCCCTCCCT TGCAAGAACC CCTACTTATC CTTTATGATC TGTTCAAATA 1440 TCACTCCTCT GTAAACCTTT TCTCAAGTGC CCCGGCCATT CAGGGAGCCA ATATTTACTG 1500 AACACCTATC ACATGCCAGG CTCTGAGCAA GGCACATATT TATCTACTCT CTCCCCTGTG 1560 CTGCTCCATG CAAACGTCCC AGGCCTGCCA GCGAGTGGTG TCTGGCCCTG TGCCAGAACT 1620 CCCAGACTTG GCTCAATAAT CACTAAATGT GAGAACCAGT CTCCATTGGA ATCTCATCAA 1680 CAGGAAGGGC TGGGCAGGTT TCTTCTCATT TCCTTGCCTT AGCTCCCACC TCAGCAGCTT 1740 CTGTGGCTAT AAACAACAAA GGACACCTAG TGTGGGAGCT TCCCTGGTCT GTGAAACAGT 1800 GTTCTTGATT CATGGGGACA TTGTGATCAG CTTTTACTGC AGTGCATTTT CCATATTTTG 1860 ACTTATGGAT ACCTCAGTGC ATGGCCTATT TGTATCTGGG CACCAGATGA TTTTTCCCCA 1920 AGAGTCATTT GCTTTGCTGT AAGCAGAATG GAAGTAACTG AGAGAATCTC TTTGGGGGAT 1980 ATTCCTCTTA GAGTAGAGAC ATATGTAAGG TGGCAAAAGC ACTCAGTCAG GGGCTGATAT 2040 TTAGTAAACA AATATTTCAT GAGATGAGTG CTGGGCCAGG ATATGAGCTA GGCACTGAAG 2100 GACAAAGATG AACTTGGTCC CAGCCCTCTG GAATGTCAGA GCTGCTGTTC AACCTGCAGT 2160 GGAGCTGTTT CCCTCACCCT CCTCTTGGCA TTGACACTCT CACTCATCTT TCAGCTTCAG 2220 CCTAAGCCTC CCCTTCTCTG GAAAGTCTTC CATGGGGCCA GCAGCTATGA CAAGTTGTCT 2280 ATCCAATACC TTTTTCCCTT CTTCCTTATA AATAAACTCT GGTTATATGG TATATTTTGA 2340 GTAGTATTGT ATATAGTTGA TGAATTTCAT TTCTCAATCT CCCTGTCATT GAAATGCAAG 2400 AAGTTGGGTG ATGTTTCTGA CAAAGTGCCT TAAAAGGAAA TGATTCAGCT GAAAGGTGCC 2460 CCCTATTTGC CCTCACTCAC TTACTCCCTT TTCATTTCTG GACCTCAGAT GTGATACCTG 2520 GAGCTCTTGC AGACACCTTG AACCATAAGG CAATCTTGCC AATGTAAGAC ACACTAACAA 2580 TGGCAGAGAA 2590
|
| |
|
|
|