| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05876 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:69233510-69235960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr11:69235505-69235520 | TAGTGACTCAGCAGA | + | 6.38 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_57195 | chr11:69235110-69235906 | VACO_400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I069419 | chr11 | 69233914 | 69236690 |
|
Enhancer Sequence | GGGGGCCTGT CTGCCACAGG ACTTGATGAG GAGGGGAAAG ACTGGCACCC ACCAAGCACT 60
TTCGACATGT CAGGCACTGG GCTAGGCGCT TGGCCTCGAT ATTCTTATTT AAGTTGCATA 120
ACAACCCGGT AAGACAAGGA CTACTACTGC GCCATTTTAC AGACAAGGAA ATTGAGGCTG 180
GTTGAGGTGA ATCAACTTGT GCAAAGTCCC AGAATCTCCA CCCGGGCAGT ATTGCCTGAG 240
CTCTTGCTCA GCCAACAAGC CCCACTACCC CCACACACCC ATGGGCCTCT TGCAACAACA 300
CCTTCCCCAC ATAGGGTCAT GGGGAGCCTG AAGTGTGCGG GGGCAGTGGA GGGCATCTTT 360
CTGAGGGCAT CCTGCCCCTG AAGCCCAAGG AGGAATCACC CTCACGGCTC ACCGAGAAGG 420
ATTGGCAACC CTCAGTCTTG TGGACTGAAG ACTCATTTCG GAGCCACTCC AGGGTTGAGG 480
CAGAGTGTGC TCCCAAGGGG TGGTTGTGCC CTGGCTCACG GCCCTGAACA CAGTAGGTCT 540
TCAACTAATA CAGCAGGAAG AAATGGTGCC AGGACAGCTC TCCACGTTGG AAGTTCTTCC 600
TTGTTAGCCC AAGCCAGGCT CCTTTGAGGA TATCATTCAG ATTATTACTT TGCTTGGGGC 660
AGGGTCCCAG GCACAGCTCC GGGCATGGGT GCAGGGATCA CACTGGACAC ACCAGATTCA 720
GACCCTTCCA GAGCCCCTTC CCTGCTGCAG GGGGCAGAAA AGAACAGATA AGCGATGGTG 780
CATAGTGGGG CAGCAGCTAC CCCCAGACTT AAGAAGAGGA CCAGGACATT TTTCGGGTTT 840
CTGGTCAATT AAATGGAACG CCAAGCAGAG TCATGTTCTC AGCATCTATG TTTAACAAAT 900
CTATACTTCA AATGCACACC CTCTCTGCTG AAAGAACACA GTCCCATCGA AGTATTTTTG 960
CCTGATGGGA GGGATTAGAA TTTCCGTGGC AACATTACAT CACTTTAGAC CAAAGCGACA 1020
GTGTCTGGGA AGACAGAGCT GGTTCTGCAC GTACCTCCGC TCCACAGTCA CGGACACTGA 1080
GGTGCTCAGG GGTCGGCGCT CAGGATCACT GGGCAGCCGT ACGTGTCCCA GGCAGCGGGA 1140
GCCCCGGCAG TGCCAGCTCC CACACCATCC GGCTGTGACA ACCTCAGGTC CTTGATGACA 1200
GGGAGCCTCT GCCAAGACGG TCCGAAAATT GGGAAGGGGA CCCGCTCATC TTTGTGGGGT 1260
CCCCAAGAGC TTCAGATAAG TTTGCTGAGC ACCGGCTTCC TGATCACATT TCACATTTGA 1320
CCAAACGATG TTCCTCTGCA GCCTCCCTCC CTTGGTCCCC AAATTGGCAG CACTTTCTAG 1380
AAGCTAGATG CAGAGGATGT CCTTTGTCAA GGGAAAAAGA AGTGTTTCCT TTGGGATAAA 1440
AGGACACACA CACGAGTGTT TATGCACATG CAGATACGTC TGCCTCTCTC TATGGACATG 1500
TATAGAGATT TGGTTGTTTA TGCATAAAAT ATCCCTGCAT GGATACCCAG GAAACTGGTA 1560
ATGTCAGTTG CCTTTAGGGA GGAAAACTAG GGGTCTGGGA GTCTTAAGTA GGAGAATTTT 1620
TTAACCATAT TTTATATTTT TTTAAATTGT TCTACTCTGA GAAAATTTGA AAGTGTATAA 1680
AAAGCAAGCT CTGAGCCCCT TGTCTTCAAC CCCGGGGCCT CTCTTGCCTG AAGTCCTGCC 1740
ATGAAGATGA ATCTCTGCCT GTACCCAGTT CCGTCAGGGT CCTGCTAAGG GGTGAGCAGA 1800
GGACACCACA CCGAGGGGCC ACCCATTGTC TCCCAACCTC GGTTCCCAGG ACTCCCGTCC 1860
CCACGGGCCC TCTAGACTCT GTGAGGCTGT GATTCTGGGC AGGGTGAAGC CGGACATGCC 1920
GCAGGGCCGA TGCCGGCCGT TGTGGAACCA GCCCTGGAAT CTCAAAAATG TCCTGTGGTC 1980
AGGCCTGAGC TTTGTTAGTG ACTCAGCAGA AAGCACCCAG CCCTGGCCCC GTGGCAGGTA 2040
GGCCAGCCCC AACCTGGGGT GCAGCCTCAG GCCTCCAGCG TCCAGAGCCC AGGCCTGTGG 2100
GGATGTGGGC CCAGTGGGTG AGTGGCCACT GTCCAGACCC TCTGTCTCAG CGAGGCATCA 2160
AAGGCTGGCA GAGTTGGCTG CTGGGGGAGC CCCTGGATGG GGCCAGAGCC CCGGCTCTGG 2220
GCTGAACTGT GTCCTGACCT GCTGACTGAC TTCCAAGGCC TCAGTTTCCC CATTCACAGG 2280
AGAAGACCAA CTGCATGTAA GCAGAAGCCT GACATTAGAA ATGCAGCTGT TCTGTGATGC 2340
AGGTGGCGTG CTTGTCAAAG GAGGTTGACA AGCCTCCCAG GCTGCGTGGC CACAGGCAGC 2400
CTCCATGCCC TGGAGCCCCA GTTTCTCCTC CATGAAATGA GGCTAATAAG 2450
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