| Tag | Content |
|---|
EnhancerAtlas ID | HS184-31614 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr9:129394780-129397420 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr9:129396336-129396354 | GGGAGGGAAGAAGGAAGC | + | 6.05 | | EWSR1-FLI1 | MA0149.1 | chr9:129396325-129396343 | GGAAGGCAGGAGGGAGGG | + | 6.64 | | PLAG1 | MA0163.1 | chr9:129395114-129395128 | CCCCACTGGGCCCC | - | 6.36 | | ZNF263 | MA0528.1 | chr9:129397219-129397240 | TTCCCCTCTCCTCTCTGCCCC | - | 6 | | ZNF740 | MA0753.2 | chr9:129396878-129396891 | ACACCCCCCCCAC | + | 6.82 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGTGGGCAGG AGGGAGCTAT TGAAGGTTAT TGGACAGGGG AGTGACAGGA ACTGGAGAGG 60
CACTTTATGG AGCTGATGCT GGCAACATGT GCCTGGGATT AGACCGGCGG GAGGAGGCTA 120
TTGCCACCTT GGAGGTGAGG GTAGTTGCGG GAACCAGAGA GGGAACAGGG CACAGGGAGG 180
GTCACAGAGG CCTGGGGCTT GGAGCTGGGG TGGCTGGAAC CCCAGGTACT CAGCTGCCTG 240
GCTAAGGCCT TGAGGTCCTG AGCACTCTGG GCTGGTCCCA GCAGGGGTGA CCCACTTAGC 300
TGGGTCCCTG GAAGAGCCGG CTTGACCTGT GCAGCCCCAC TGGGCCCCAC ACCCAGAAGG 360
GCCCTTAGCT TGGTTTAATG CTCCTGCTGT CACACTCTTG AGATTCTTAA CTTTTGAACA 420
AGTGGCTCTG CCCCTGCCTT TTCATTCTGT GCTGAGCCCC GCAGGCGAGC CCCCAGCTCA 480
CCTGCCATTC CCACATGTCC CAGACACTTG CCCACATCAA GGTCTTACTC AGGCTGTGGT 540
GGTTGCCCAG GAGGCGTCCC CTGGCCTCCA TCATCCTTTC TTCTTCTGGA AAACTCTCCC 600
TACTCCCAAG GCCTGGCACA AGAGTCACCG GTTTCATGGA GTCTCTCTGG CTCTGAGCCC 660
CACCCCCGTC CTCCAGGCTT GGATCTGTCC TGTAGCACTT GCTAGAGGTG CAGAATCCTA 720
GATCTGTGAG GGAACTCGAA CTCTCGAGGT GAAGCCCATG AGTCTACATT TCCAGATGGC 780
CCCTGGGGGA AGCCTTGCCT GCTGAGGTAT GACAACCTCT GCCCAGGGTA CCTCCAAGCC 840
TGGCACAGGG CCTGGTACTT GGTAGGTGCA TCCGTGTGTC ATGTCATTGT GAAGGAATGA 900
ATGAACGGTG CTTACCTGTC CATCTGGATG GATGAAGCTC CCTGGGCCTA GCTCATTGCC 960
TGGCATGGGT GGGTGGGTTG CAGCAAGTCT CCACAGGACA ACTGGGAGGA CACCTGGCCA 1020
ATCCTGGGGA CTGGCTGGGG CAGGGTTCTT CTTCTTCCTG AAACCTCGGG ACATGGGGGC 1080
CAGGCTGGGG GATGGAAGGG CAAAATTAGT ACCCTCCGGG AGATGGGAAG TGGGCAGAGG 1140
CCACGGAGTC CACCAGCACA TCCTCCCTGT AGCTGTCCCC TCCTCCGAAA GGACTACCCA 1200
CTCCTGACAT GGTTATACAG CACGCACATA ATTATACAGC ATGATGGAAG AAGAGAATTT 1260
GATTGTTATT TCCAGAGCCT TTACCCTGTG CAGCCACTGA TTTAAGGATC ACATTATTTC 1320
ATTCAACCGT AAGCCTCATA GTCTGTGAGG CAGAGCCTGT TATTATCCCC ATTTCAGCGA 1380
TATGGAGACT GAGGCACAGA AAGGGGTAGT CGGCAGTCCA AATTCACACA GCTTTGTGTG 1440
ACCCCTCTGC CAGTTGGCCT CCGAGATGCC TCATTCCCCC TGTGCCTCCC GCTTTTGATG 1500
CCTCGGGGAT ACACCTGGCA CAGTATGTAC TCAGCGAATG TTTGGGGAAG GCAGGAGGGA 1560
GGGAAGAAGG AAGCCCAGCT CACTCATCCA ACCGGAAGGA CCCCTGCTCC AGGCAGGACT 1620
GGAATAACGC CAGGACTCCA AATGAGCAAG ATAGTCCCAG CCTGGCCTGC CTGGGATAAG 1680
GAGCGGGCAG GGAAACCCAG AGGAGAAGCA CTGACTTTGG CAGGATGGGG CATGTGAGGG 1740
CACCTGGAAG GCACTGTGGT GAAGCCCGGG ACTGGAAAGC CTTCTTGCCC AGCAGTGACG 1800
GGGTCGCCAT GGAGAGGCCT CACCGGGCAG GTCTCTGAAG CCAGCGTCAG TTTCATACAG 1860
GCATTCCAGA AATACATGTG GAACTTCCTC CCTCCACGCC CTGTGTGGGT ATCAGGGAGG 1920
CATGGGGAAG AAAACGCTCC AGGTCCTGCC CTCGGCTGCC ACCATGGTGC TGAACAGGGT 1980
GAGTCTAGCC AAGGAGATGC CAGGAGCAGA CCCGGTGCAC AGTAGGTGTT CAGGGACTGT 2040
CCCCATGGAG ATTTTCAGTT ACCCACCTCC TGCATTAGCC TCTGGTGCCA GGTTCTGCAC 2100
ACCCCCCCCA CAATGCCACA TCCATGAGCC ACTGTCTTGA GTCCTTTGAC CTCTCTGAGC 2160
CTGAAGTTAG TCATCTATAA AATGGGTACA GCTATTCCTA CTGTCCAGGT TGTTGTAGGG 2220
ATTAATTTTG TAGCGATTAA TCCAGGGGAG GGCCCCGCTG CGAGTGTACC TGGAAGAAGG 2280
GGTGCTGCCT GGAGAGGTGG GAGAGCTTTT ACCAGGCAGG TGACATTTGG AGTCACGAAA 2340
GGGGAGGAGG AGGGCTTTGC AGGTGTGGGG TACAGTGTGG GCCAAAGCCC AGAGACATGG 2400
AAGCCTGTGG CCTGTTAGAA GCACAGGGCT CCCCGCTCCT TCCCCTCTCC TCTCTGCCCC 2460
TGGCTGTCCT CTCACCCTCA AGCCGGTGCC AGTGTGGCTC TGCAGATTTG CTTCTAAGCC 2520
CTAGCACCCG CTGCATGCCA GCCAGGCACA AGCGCCATAT GAAGCCTGCT GATGGCCTGG 2580
GAGACAGGTG TTACTGTCAT TCCCATTTCA CAGATGAGGG GACTGACACC CAAAACCCAG 2640
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