| Tag | Content |
|---|
EnhancerAtlas ID | HS183-14719 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr9:140358900-140361760 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr9:140360050-140360061 | GGTGACTCATT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTCATGCCCT GGGGCCACAT GTGGAATTTA CAGAAGGCTT CCACCCTCCC TGCGGGCTGC 60
CACAGCAGAC ACGTGGCGTG CTGAGGGCCT CTCATGAATG GAACGGGGGT CCAGAGTGTC 120
CTTGGGCCCC ACCCACGGTC CTGAGGCTTG GCGCCCTGGC TGGAGCCTCA GAGTGAGCAG 180
AGGCTGGTGG TCGCCCCAGG GCCTGAAAGC CAGGACACAG CCCACCCTCG GTCCCTTCCT 240
GATCCCTAAG CCCTCGCTGG CCCTACCCTC GCAGGCTCTG CAGCGCCCCC ATGCCTGGGG 300
CCTCCTCGGC TTTGCCTGCT CAGCTCTGGG GCAAGGCCTG CCCATGCCCG TGGCTGGAGG 360
GTCAGCGAGG AGGAGAGCTC GGGGCGGGCT GCTGGGCACA TGAGGTTCCT GGGCCAGGGG 420
GACACAGTGG ATTGCTTTCG GGAAGGTCAG AGCCACCCAG CCCTGGCTCA CATGCCACTG 480
CGGTACTCCA TCAGGGGTCC CGGGGAAGCC GGGCTCTCTT GGGTTCCTTC TGGGTGGGCC 540
TGGGGCCCAT CCTTCCTCAG TGAGGCAGGC AGGACTCGAG ACTGACCTCA AACTAGCCTC 600
AATGCCCAGT GTGGATGGAG AGGAAGGGTC TTCCCTGCCA TAGTGAGCCA GGGCTCAGGG 660
GACGGAGGCT GGGAGGGAAG CGCTTGGAGT GTGGGCTGGA CGTGCTTACA CCGTGTGATG 720
CAGGCAGTGA GAACGCCTCG GCCACAGGCA GAGGAGACCC CGGTCCTTCC CTGAGGAAGC 780
CCCTGCCCAG TACCAGAGGG GCTCACAGAG ATAAGCCAGA CCACACGCCC ACTGTCCCCT 840
CTCCTCAGCA TGAGGGGCAG GCACACAGCC CCGGCCTCAC CTTGCCCCGG CCAGTTCCCA 900
GGGCCCAGTG ATCCCAGCAC GGAAAGAGGA CCAGCCCAGA GAGCTCTGGC CATTCCCACA 960
CCTGGCCCCC CAGCCCCAGA CCCACAGACG GAGGGACAGG GAGAGGGCCA CCAGGTGACT 1020
CTGGGACAGG ACCGGCTCGG AGCCACCTCT GCCCATGGCG GGTTCTGTCC CGAGGACGCT 1080
GTCCCTGGGG CCGTCCTGCT GCATGCCAGT CCCCAAGCCC TCTTTTGAGC AGCCACGCTG 1140
AAGGTGACTA GGTGACTCAT TTTAGGGAAA GAAACATTTC TGAACAGAGA GGGGAGAAGG 1200
TGTCAGTGGC CTTGGGACTC GCTGCTGGGG CTGGTGGCAG CCCCGGGCCA CGTGAATGCA 1260
GCACAGGCCT GCTTGGGAGC TGCTGCCGCA CAGGGGGTGA CGAATTTTCT TTCCTTTTAA 1320
AAGGAGAACA CGAACCCTTC TGATCCCACT CATGGCTCCA ACCAAAGCTC GGTTTTGTTC 1380
CACAAAAGCA AGCGCAGCGC TGAGGAGGGC AGACGGTGGC CACGTCTGCT GGGGAACGGA 1440
GCCTGGCTGC CTCCCTCTGC TGCCCGAGGG GAGCCTGTTC TCACTGTTGT CTTTGATTCT 1500
GTATTTGGTA TTCTGATTCT GGAATCCATT TATCACAAGG CCAGACTAGT GGCCAAAGTA 1560
GTTTACATCT CCCCCGTGAC ACTGAGCCGC CCTGACCTGA TCTCACATCC CCACGCCAAC 1620
ATCTCCCTGC CCTAAATCAA CCCAGGCCGG GTGCCATGCA CCAGGGACAG CCCCACGGCC 1680
CCCAGCGTGC CTGAAGGACT CAGTCAGCCC ATCCTCAGCT GCTCACGCTG CCCTGCCTGG 1740
CCGTTGGGTC AGAAACCCCC ATGGAGGCTC CATGCCTCTT ATTCCCAGGG GCTGTAACAG 1800
TCAGCTTCTT TTCCACAATC CTGGCATCCA TGTCATCCTG CAGCCACCTC CACCATCTCA 1860
GACCCGGGCA CGGATCAGAC CGCCTCCCAT CGTCAACCTC CACCAACTCA GACCCGGGCA 1920
CAGATCAGAC CACTTCCCAC CACCATCTCC ACCATCTCAG ACCCGGGCAC GGATCAAACC 1980
GCCTCCCAAC ACCGTCTCCA CCACCTCAGA CCCAGGCACA GAACAGACCA CCTCCCACCA 2040
CCACCTCGAC CATCTAAGAC CCGGGCACAG ATCAGACCAC CTCCCACCAC CATCTCCACC 2100
ATCTCAGACC CCGGCACGGA TCAGACCACT TCCCACCACC ACCTCCACCA ACTCAGACCT 2160
GGGCACGGAT CAGACCACCT CCTACCACCA TCTCCATCAC CTCAGACCCG GGCACGGATC 2220
TGACCACCTC CCACCACCAT CTCCATCACC TCAGACCCGG GCACGGATCT GACCACCTCC 2280
CACCACCATC TCCACCAACT CAGACCCGGG CACGGATCAG ACCGCCTCCC ACCACCGTCT 2340
CCACCAACTC AGACCCGGGC ACGGATCAGA CCACCTCCCA CCACCGTCTC CATCACCTCA 2400
GACCCGGGCA CGGATCAGAC CACCTCCCAC CACCGTCTCC ACCAACTCAG ACCCGGGCAC 2460
GGATCAGACC ACCTCCCACC ACCGTCTCCA CCATCTCAGA CCCGGGCACG GATCAGACCG 2520
CCTCCCACCA CCGTCTCCAC CATCTCAGAC CCGTGCACAG ATCAGACCGC CTCCCACCAC 2580
CGTCTCCATC ACCTCAGACC CGGGCACAGA TCAGACCACC TCCCACCACC GTCTCCACCA 2640
ACTCAGACCT GGGCACAGAT CAGACCGCCT CCCACCACCA ACCTGCATCT GTGCCTTCTC 2700
TGTGGTGCTC CTTTGCCTCA CAAGCTGCAC TGGGAGGCTT CAGGGGGTAG CCTCCTCGAG 2760
GGCAGGGCCC TGCAGAGCCA CATGCAGAGG CCAACGGCCC CAGCGTCCCC CAGCACCAGC 2820
AAGGACCTGG GGGCTGTGCT CCGGTGAGGG TGATGGGTGC 2860
|
| |
|
|
|
