| Tag | Content |
|---|
EnhancerAtlas ID | HS184-30666 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr9:5843340-5844250 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr9:5843908-5843929 | GGGGGAGGAAGGATGGGAAGA | + | 6.79 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_33805 | chr9:5842266-5847724 | HCC1954 | | SE_35681 | chr9:5842755-5845125 | HepG2 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I005841 | chr9 | 5841318 | 5846255 |
|
Enhancer Sequence | TGGAAACAAA TTTAAAAAGA GAAGAACATT TTGTGTGCCA AAGAAAATAG GTGTGTAAAC 60
TGGATTCCAC CCACCTGCTG CCAGTTTGAA GCCTCTGAGC CCTCACCTTT AAGCCCTCAA 120
GGACATACTT GATTAAAGAT AAAATATTTC CCTGAGTGGG GATCAGGTTA TTCATGAGAT 180
TCTTATCTCC AGATTTGGGG GAAAGTTTAT AGTGCTAGAA TGTATCAGAT GTAGCTAGCC 240
AGTCAAGTCT CTTTCTTCTC TCCTTCTTAG TTGAGAGGTC AGTCTTGTCA AATGCCCCCC 300
TCCCCGCTTC TAGCCACTGC TTTGTTTATT TTGCAGGAAC AGTGAATAAG TAGCAGAACG 360
CTTTCTGAAG TTTTTGCTGA TGCAGAGCCG AAGATCTCTG CTACAACAAA TGTTCTGAAA 420
TGGAGTCTTC TCTCTCATCC CCATCCCCTA CCACGGACAG TGTTGCACAC ACCGGGGTTG 480
TAAAACTCAA AGGCAGAGTT ACAGCCCTCC TGGATTTTAG ACCAAGCCTG GGGATATGCA 540
GCTGTATTTA CTCTTCTTGT GTGTCCTGGG GGGAGGAAGG ATGGGAAGAG CAGTGCATCC 600
TGGAACCGTG GCTATGGAAA ATAACGAGCA CTCCTCCACC CCCTGGCCAA TACCGGCACA 660
GACTTAATTT GAGGGGTAAT GTTCTGTGAA GTATGATGGC ATTTCCGGGA GAAGAATCTC 720
AGTCAGACCT ACAATCAAAC ATACATTTCC TTACCAGGGG TAAGGAAAAA AATCTTTCCT 780
CTTAAAATTA GACACCCTGT CCTGGAAAAC ACTAACATCC TACATCCTGA GACTTCCTTC 840
CTGCAGCCTT CCAGCTCTTT CTGCCCAGAC TCAGATGTAA GTGGCCAAGT AGCCACAGGC 900
TGCCTAGCAG 910
|
