| Tag | Content |
|---|
EnhancerAtlas ID | HS007-04227 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr12:120538220-120539590 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:120539302-120539323 | ATGCAGTTTCAGTTTCTCTCT | + | 7.22 | | IRF9 | MA0653.1 | chr12:120539306-120539321 | AGTTTCAGTTTCTCT | - | 6.28 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27057 | chr12:120537449-120541185 | Esophagus | | SE_31982 | chr12:120538202-120540645 | Gastric | | SE_41982 | chr12:120537882-120541422 | LNCaP | | SE_68937 | chr12:120538843-120541016 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I120099 | chr12 | 120536948 | 120540903 |
|
Enhancer Sequence | GAAGAAAGGA GCTAAGCATT ACCCCAAGGC GGGGGAGCAG TAAACAGTCA GTATGCGTTC 60
TTCAGCATCA TCAATGTGCC TTCAAGGACA ATCTGTGGTC CCAGACAGAG GTGGTGGAAG 120
GAAACCAACA GGCAGCTTAG GGGCAGCCCT GAGCATCTTC CCTGATGCTG CAGAGCCAGA 180
GCTCCTGCCC AGCCCTGGGA CAAAGCCCAA CCTGCCCCTG CCACCGCCCC TGCCCCATCC 240
TTGCTCCATC CTCAACACGA CCGCTGGGAT CTCTTCCCAG GGCTTCATTC TGCCCACAGC 300
TTTGCTTCCA GGGCAGCGTC GCTCCTTGGC TTCGGGGTAG CTGTGACGAT CAAGCTCTCT 360
TGGCACTGGG CCCAAGAACT AGCTCTGGCC TTGGCAGCTG CTGCTGAGAG CGCCGGGTCA 420
GCACATGGCA TGGTGTGTCA GACGCCTTCC AGAGCGAGGG CGCGCCGGAG CCACAGGAAC 480
AGGCGACTGT CCCCTGCCAG CAGAGGAAGC CCAAGGAGCG GATGGCTCTG CAGACTCTCC 540
TTTGCTGAAG ATGATCAGAG ATGCCAAGAA ACGCCTGCAG CCATGGCCCC GGCGCACAGC 600
CCCCGCGGCT CCCTGGGCGC CTCTGCCTCA TCCGGGGCCC AGGAAAGGGG CTTTATCTGA 660
GAGCAGAGAA TTTGTCTGGG GATGAAGTCA GGGGCTCAGA GCTCTGGCTA GGAGGAACCG 720
GAGCACCGAC GTTTCCCATG GCCACCAGGA ATCACCTTCA CTCACAGGGA CTCTGCTCTA 780
GGCCAGGCAC AGAGCTGGGG GCTTGGTATC CATTACCTTA TTAATGTCTG CAGCCACCTG 840
ATCCAGCAGA CCTCAGGATG GCCATGTGAC CAGCAAGGAC GTGAGGCTGA GTGCAGCGGC 900
CAGCTGGAAG TCCTGGCGCC CAGGGCTGAC TCCCAGGCCC AACGCCAGGG CCTTGCCTTC 960
CTTGTCACTT CTCCCCTCAC CTCCATCCCA CCCGCACCTC TCAGGGCCGG CAAACCTCAG 1020
CTTCTGAGAG CAAGAACCCG AGAAGGGGTG ACCACAAGGC TTTTTCTCGC CAGGCTAACA 1080
GGATGCAGTT TCAGTTTCTC TCTGAACGCC CTGCATCGGA AAAAAGTCAC GCTACTGCAT 1140
CCTGACTGCC CTATTCCTGA AAACTCCTCA CCTCCCCAAA ACTCCTTCCT TCTTTGCCAG 1200
TGACCATCAA AGGGCGTCGA GACTTCCAGT GGCCCCTCAG GGCGCCCTGC TGGGCCTCCT 1260
GCCTCATGAG GGCCAGAGCG GGACTCTAAG ATGGAGCCAC CTGTCTGCTT CCCCAGACAC 1320
GTGGGACGGC AGCAGGGGCC CAGCCGCTGC CCACAGGCCG CCCCTTCCCA 1370
|
