| Tag | Content |
|---|
EnhancerAtlas ID | HS183-05103 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr5:884180-886700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr5:884637-884656 | TGGCCACTGGGTGGCACAA | + | 6.38 | | HSF1 | MA0486.2 | chr5:884751-884764 | GAAGGTTCTAGAA | - | 7.12 | | MYC | MA0147.3 | chr5:886518-886530 | GTGCACGTGGCC | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGCAGCTGTG AGGTGGGGAC AACCAAGTCA CCTGGAGGCA GCGTCCCCAC CGCACACCTG 60
CTCCCCATGC GTCGGCACCT AACCCAGCTT CTACCGACCC TGCCCTCAGA CACAGAGCTG 120
GCAGAGCATA CTTAACTCCT TTTAGGTCTC AAAGCATCCC TTTTCACCCT AACCAAATGA 180
CAAATTAAGA CACTTTTATT AAAATAAAGG GTAAGTGTAA GCCAAGTAGA CAGACTTCCT 240
ATTTTTCAAC GCAGTGCAAA CTCAGTTAAA GTGCTTTAGC AACAAAAGCA ACAAAGTAAC 300
AGATGCCCAC ACTGGTTAGT TATTAAAGGC CCCATCAGAA AAGTGACTGG AAAAGCCACC 360
CCTGACTACG CAGGGTTCAC AGCAAGGCAG GATAGGCGGG GCTGCTCGGG TGTGGTCTGG 420
TGCTGCTGGG CTGGGTGGAC AGCAGCCCCC TCTGCTGTGG CCACTGGGTG GCACAAAGAA 480
CACACAAGGA CGTCAGCAAG TGGTCCCAGG TTCCACCTGA AGCAGTTCTC CAACAGCTGA 540
GGGGCACAGG CTGTAGCACC CAAGGAGTGT GGAAGGTTCT AGAAGCAAGC GAGTGGGCTC 600
CTTCCCACCC TGGGCACTTG CCTGGGCATG GGTCTGAGTG GCCTAGGGCC AGGTGCAGGC 660
CCAGGACAAG CCCTGCCCAT GAGAGCGGCC CTGCCCTTGC CTGACCTACA GTGACAACCT 720
GGCAACCCTA CACAGGAGTC ACAGCCCCAT GAGCTCCGCA GGGAGGGGCT CCACTCAGGC 780
ACCTGCGTGA GCCCATTACC GATGCGCACT GCTGTGACAC TAGGTGAAGG TGACTGCCTG 840
AGCTCGGCAC GCTCTCCTGC CTGCAGACTG ACAGCTGGGG ATCCATCTAA AGGGCCTGGA 900
TCCCACAGGC AAGGGTGAAG CTGCAGCACC AGAGACACCC AAAACCAACC TGGGGTGGGT 960
CTGCCAGGAC ACAACCCCAC CGCAGCTGAG CATGCTGACC AGCACCAACT TCAATTCCCC 1020
CTCGATGCTC AGTCACCATG AGGCGGCAAA GGGCGGCCAT GAAACCCCGA CCCCTGAAGG 1080
CCAGCAGCAC ACTCGAGTCG GGGGCTGAGG CCGGACACAG CCACCAGCCA ACCACGCAGT 1140
GAGTGTTCAC ACGGCAGCGG GGTGGGAAAT GCAACGCACG TGGGGAGACC GCCTTAGGGG 1200
ACTGTCGTCC GTTGCCAAGC AACACACTCT GGCCACGCAG CGCACCCTGT CTCCTAAGCC 1260
AAGGCTGCAG GACCTGAGGG GCTGGTCTCA AGACCACTCT CCCTTTTGAC GGTTGGAGGG 1320
AGCTGCTCAG AGCAGAAGCA CCGAGCCCAG CACCGCTGCC GCCCCACCTG TTAAATCCAC 1380
GTGAGTCCCA TACACATGTG AGAAGGAAAC AAACAATGGA GGGCCGTGAC CATCACAATT 1440
GCCTCAAGGA CGTTCAGTAC CAACTCCAGA CGGTCCCTGA CTTCCCACAA GATGGCACAA 1500
AAGCAATACA CTTCAGCAGA AACCATCCTT CAAATCTGAT CTGTCCCCAG GATGGCAACA 1560
GGCCAGTCCT CTCAGGATAC TGGGAAGACC GCGAGCCACA GTGCTGTCAG ACACACGGCC 1620
ATGAGGGTGG ATGTCCTGAG ACTGCGCTCT CTGGGGCCTG CACTCAGCAA GTGACACGTG 1680
ATGAAGCAGG CTCTGTGCCA GGCGCTTCTG CCCGCTGCAG GCTATGTTAA GTGCTCTTGG 1740
TGCCTCTAAG GCCCCTGGCG ATACTCTCGC TTTGTTTGGT CCTATCAGGC AGCCACCTCA 1800
CATAGGTGGA GGAGCGTCTA CAGGAATGAC GTGTGATACG GACTTTGATA CAATCTCAAT 1860
GCTCAGCCAC CATGAGACAA AGAGCCCCCA TGAAAACCAC TCTGGGGTTT AGAAAAAAAG 1920
GAAGAAGGTT CCCTGAAGGA CCAGCCAAGT CGGCTGCTCC CTGTGGGAGG GAGCAGAGCT 1980
ACAGGGAGCT GTGGCCTGCA GTCCTCACCT GCTTCCCCCG CAGCATCCAC ACCTTCCTGA 2040
CCACAGGCCT GCACCTGCTC CACTCCAGCG TCTACACAGA CACAGAAGCG AGCAGTTCAG 2100
GAGTGTGCAT CTGCCCCACA GCAACAAAGA AGCCCCCTGC CAATGCTGGC TGCCCAAAGT 2160
CAGCCCGCTT GTGCGGCACA GTCTGGGACA AGGGCACAGC CTTGGCTGCC GGCAGGCGCT 2220
GTGCAGGGGA GGGAGGGGCC AATGATCTTA ACGGCGTGTA GAGACAGAGA CCACCAGTCA 2280
CTAGCAGTTG GGGGCAGGGG TGATCGGACG GGCTTGGGTA CCACACCTGG GTCAGAGAGT 2340
GCACGTGGCC GGTGGGCAGG AGGGGCTGTC TGGCCACACT CCTCCTGCCA GAATAAGCTA 2400
CACCAAGAAT GTCTATGTGA CATGACATCC GTTCTCTCAC TCACTCACTC TCCCCTACAA 2460
GGCACCTGCT TTCCTGGCTA TGGTGCTCAA CTCCAAAAGC AAATGTGGTT TCCACAGAAC 2520
|
| |
|
|
|
