| Tag | Content |
|---|
EnhancerAtlas ID | HS183-09685 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr7:50660790-50663130 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr7:50660937-50660948 | GGGCGGGAAAG | + | 6.32 | | HLTF | MA0109.1 | chr7:50661842-50661852 | ATATAAGGTT | - | 6.02 | | IRF1 | MA0050.2 | chr7:50661669-50661690 | CCTTTCTTTCTTTTTTTTTTT | + | 6.1 | | POU2F2 | MA0507.1 | chr7:50661833-50661846 | TGTATTTGCATAT | + | 6.41 | | RORA | MA0071.1 | chr7:50662777-50662787 | TGACCTTGAT | - | 6.02 | | Stat6 | MA0520.1 | chr7:50662945-50662960 | TATTTCCAGGGAAAT | + | 6.12 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41576 | chr7:50660328-50661230 | LNCaP |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I050592 | chr7 | 50660329 | 50661230 |
|
Enhancer Sequence | TCGCACTGGA GAGACACAAG AACACTTGCC AGGTTAGAGG CTGCCACCTC AGGGAACAGA 60
ACGGGGCCCA CGGCCAGCAG CAGCTACATC TGCCCATGAT TTGATTCCAG AGGGACACAC 120
AGGGCAAGGT AGGCTAGAAA ACACCAGGGG CGGGAAAGAC GGGAGCAGAG GATGTGTGCT 180
GGGGGCTGCC ATGTCCCTGA GCGAGGGACA GACTTTGGGT GGGCTGCGGA GGCTGCTGAG 240
GACAGCTAGC TCCCCTGCTC CCTAAGGTGG TCAAGGGGAA GGGCTCGAAG TTGCCCCCAG 300
TTCACCCAGC TCATGAGAAT TACATTTACC AGTTAACTTG TAAGTACCCA CTGCACACAG 360
CATGCCCCGA GAAGACTGCA CAAACCTGGG TCCTCACTAT ACGACCTCAG CCAACTCCTG 420
AGGCCCCAGG GGTTTACTCT GCTCCATGAT GAAGCAACTG TTGGGTGGCT ATGAGGGATT 480
AATAAGCTCA CGCAGGTAAA TTCCGTTCCT AGGTCCCTGA ATATGGGGCA GTTATTTTTA 540
TTAAAGCAGG GGAATGCCAC AGTATCTCCC AGAGAGAATC ATATTCCTAA CACCTATTTT 600
AACTCAGTGA GTTTTCAGTT GGATGACTGT AGTACAGTGC AAAACACTGC TGAAAGGAGG 660
TCGTGTTGTT CACAGGGAAT AGGTCAGCCT TAAGGCTTGG CTAATTAATG AGCTTGGAAC 720
CACTTCGTAA CTCTAAAACC ATTGCTAGAG CTAACAGCAC ATCCCACAGC CAGTTTTCAC 780
ACACAGAGGC TGCACACCTA ATGCCCTAAG TCCCAAGTTG CTGTTCTTTT GTTACTTGTA 840
GGATTTGGGC ATTACACACT CTGCCTACCA CGAAAGCCCC CTTTCTTTCT TTTTTTTTTT 900
TAATTTACTC ATCCAGCCTA AAATGTCAAT CACTTTTCAT TTTATATTTT GAGCTAAAAG 960
AATTATAACT GTGTGAATAA TATAATGCAG TAGAAGAACA AAAAGGATTG TCTATGCAGC 1020
ACTTTCCCTA GGACAGTAAT TCCTGTATTT GCATATAAGG TTGGCTGGAA GCTGGGAAGG 1080
CTGGGCTCAA CCCCAGATTC TGTTCCTCAC CCCAGTGCGG TGCAGGAAAA GCCACTGACA 1140
GCCATGAGCC TCATTTTCCT CACGAGTAAG GTGGGGATGT CAGCACACAG CAGGAAGCAA 1200
GCAGCCACAG AAAAGACAGT GCGTGGCACA CTGCCTTCCC CTGGCTCACA AAAGCTAAGC 1260
AAGACACCCT CCTCATCCTG TATGGTCCAT GGCTGCCAGT CACTACACGA TTCTTGAGAT 1320
CATAACAAAG TCCTGGGGGT CAGATAAGCC TGAAGAACTC CAGGTTCAAC TGTGTAAAAC 1380
AGGTGAGTTT AGTTAATTTA AGCCTTCTCA GAGCTTTTTC TTTGCTGACA TGCAGATTGA 1440
ATCTCTGAGA GGAAACTGTC CAGCCAGCCT CTTTTGGTAG AGTTTGGGTT CCACAGGATG 1500
CATTTCACAA ACATTATCAT TACCTGCAGA ATTTATCAAT TCAGCATGTA AACAGCTGCT 1560
ATTAATTTTG TGTATTGTAT TCTCAACTAA ACTGAATTCT TGTAGGCGCT GATCTAGCAC 1620
TCTAATCATG AACTAGAATT GAACTGTGGC ATACTGAAGT GAGAGGTAAA CATCAGGCGA 1680
ATCAAACATA AAGTGCTTTG TCAAAAAAAG TAGTGTTGAT TAATGTATTC TGTAATGAAG 1740
TTTTTGGAAT TGTTCAAAGG GAGAATGGTC TTTAGATCCA AGGACCATGT GGAAGGAGAA 1800
ACAAAATTAC TCTTTGGGAG GCCACTTAAC GCTTCTTGGA TAGCCCTGGT GTACACCAGG 1860
ACAAATTACA AGACTCCTCA GACTCCAGCA GCCAACAGGC AATCCTGCTG CACAACTCCT 1920
GCCTTCCAGA CCCACGTGCT CACAGCTGCT GCGACCTCAG CTAATTCTCC TCCACCTCCC 1980
CTTCCTGTGA CCTTGATCCT TCCCATCAGT ACCCTTTCAG CTGTGGGCCC TCAGCTAATT 2040
CTCCTCCACC TCCCCTTCCT GCGACCTTGA TCCTCCCCAT CAGTACCCTT TCTGCTGCAA 2100
CCAAGAGCTC ACAGGCTCAA GGGGGGCCTC AACACCCTAT CACCACTTTC AGGATTATTT 2160
CCAGGGAAAT GTTTTTCTAA TTTCAAAAGA CAAACCTGTA AAGAAATTCT TGAAAGTTTC 2220
TTAACTGCAG CCTTGAAACT GTCTGATACT TACCGGTCTT GTCGGTTTAT AACTTGAAAA 2280
TTGCATTAAG AATGAAACCA GAAAACAAAC CACAAGGACT GGTCTGAGAA CATCAATACT 2340
|
