| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05894 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:69980420-69982410 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr11:69982306-69982321 | AGGGCTGGCTGACCC | - | 6.02 | | ZNF263 | MA0528.1 | chr11:69982116-69982137 | CCCCCCAGACCTCCCTCCTTC | - | 6.42 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_01662 | chr11:69977616-69983019 | Aorta |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I070136 | chr11 | 69981721 | 69981870 | | GH11I070135 | chr11 | 69981923 | 69982368 |
|
Enhancer Sequence | AGCACTGAGC CCCCTGAGCC ACTAGAAGAT TGTTCAGTGC CGCCTGCTGT GGTCAGCCCT 60
GCTGCCCCGT GTACATTTCT ATAGCGCCCC CGGGGCTCAG ACTCCCGCTC TGCCAGTTCC 120
CACCTCACTG CTCTAAACCT CAGCTTCCTC ATCTGCAGAA TGAGGCTGCA TGAGGATCAG 180
AGGCGACGGA CATGAACTCT CAGCCGAGGC TTAGCACATA GCTTACTCTA AATAGGTGGT 240
CACTGCCGTC TTACCACATT GGAGCATGTG AGAACCAAAG AAAACCTATA CGAGAGTGTG 300
CGTGCGCCTG GTGTGTGGGA GGTACTCATC AGCCACGTGT ACTGAGCACA TGTGTCCCAC 360
CTGCATGAGG ATGTGCACGT GCCTGGTGTG TGGGAGCTAC TCATCGGCCC ATGTGTACTG 420
AGCACAATGT GTATCCCACA CTGTGCCGGG CCCCAGGGGA ACCAAGGGAA GCAAACCTGA 480
TGTATCCGCT GCTCTAAAAG CTGCAGCGTA GGTTTCAAGA GAAGGCCCCA TGGGAAGGGT 540
GCGGGGCTGT GGCAGGAGCT CCAGGTGCAG GGACCAGGTG AGAGGGGTGT CAGAGCATCC 600
GGAGAGGTCA GCAAGGACAC GCTGAGAAGA ACTTAGTGTG CTGGCTCAGA GGAATCAGAA 660
CCCAGTGCCA TCAGCTGCTG TGTCAAAGAT GCTTTCCTGT CTTATGCTCG AGTCGGAGAC 720
CGCAAGTCTA AGAGGGAGCT TGTGCAGTGA TTAAGAGAGG GGTGACACAG TGGGGGCCCA 780
GCTCCAGGAA GGGCACCTAT GGGAAGGTGT GAGAGAAGCG ATTGGGAGCC TCATGGCACC 840
CTCCCTCCCT GGCCCTGGGG ACCCTGATTT CATCCGTCTG TTTCCTCTTT CCCTGCTGAA 900
ATCCCTGGGA GGAATTCAGC CCTTAGACTC CCTGTAGCCA CTTCTCCAAA GAAAAGGCCT 960
CCGATGGAAA AGAGAGACTT TAGATTATTC CAAAGGACTC CACACTTTGT TTTAGCTCTC 1020
ATGCTATTCC CATGAGTTAA GGAGACGCTG GCGGGCTTGG CCGAGCTGGT CTCATCTGAC 1080
ACACAGGGTT ATGAATTACA GCTCCCACAT TTAACCATGA ATAAAAGGCT TTTAAGGGCC 1140
CTGGAGAAAG CAGCCACCAC GTCCTTCCAC CCCACGCTCT GCCCATCCCT GGCATCACCT 1200
TAGGATCTGG GAGGGCACAG CCGTCTGAGA ACCCCTGGCT GGTGTTCTTC TCTACAGCGG 1260
ACTCCAAAGG CACCCACTTT TGTGGGACTC TCCAAACGTC CAGTAATTCC TGGGTCCACA 1320
GAACTGGGCC TCCCTCCTCT GCAGAGAAAG AAGGACGTGG TGTTTCATTT TCTCCTTCTC 1380
CAATTACAGG CATGCCCAGT AAGAGCACAT TCCCAGGGGA AGGGAGGAGA GAGGCTGAAG 1440
GAGCCCGGAT GAAGAAAGAA GCCGTCTTGG GCTGTAATGA TCCCATTTCG AGCTTAACAC 1500
GCCGGGCGAT AAGAGGTCTC TGTGATAAGC GCCTGTTGCG GCTCTTGTTT TGGGAGCCCA 1560
AAGCGCTACG TGGCATTCTG GTCACTGCAA ATTCCTTCTT CTGAGTGCCA GAGCATCACC 1620
CAGTCACGCC TTCCAGGTCA CCTGTGGGAG TGCCTACTGG GCAGGCATGG GTGCCGCAGC 1680
CACAGAACGA GCCCCTCCCC CCAGACCTCC CTCCTTCTGG GAGTTCCTGC TGCAAGGTCG 1740
TCCTTTGAGA GGATGCAGGC AGCGCAGATT GGTCAACACC CTGGTTGTTT GGGGAGAAAC 1800
CCTCAAGGGT CTGGTCCCTC ATGCGTTGGG CTGGCTAGCA GCCCTGTGGC CCCCAGGCCT 1860
GTGGACCCTC CAAGACTAGA GCGTCCAGGG CTGGCTGACC CTGCTGGAGG CTCTAGACCT 1920
GGGCCTGATT CCCAGGGGGC AGCAGCTCTG GGCTTGTCGG TCCCCTGTGG TTCTCAAACT 1980
CGGTCCCACA 1990
|
