| Tag | Content |
|---|
EnhancerAtlas ID | HS003-12029 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr12:121340470-121341640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF740 | MA0753.2 | chr12:121341532-121341545 | GCGCCCCCCCCCC | + | 6.1 | | ZNF740 | MA0753.2 | chr12:121341534-121341547 | GCCCCCCCCCCAC | + | 6.29 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27043 | chr12:121340195-121348599 | Esophagus |
|
Enhancer Sequence | CGTCCCATTC TATTATGCTC TTTTCTAAGA AGGGAATGTC TACAGTTCTG TCCCAAACCA 60
CATTTGCTTC AAGAGTAAAC CATCTTCAAA CCATTTCTCT AAATTGCAAT CAGGTCCCCC 120
ACTCCTACGA TCATGCCATT TCTTGCTTCC TCACTCTCCA GCTATGACTT CCTTCTCACT 180
ACCCGATTTC CACTCTTCAT GGATACTGCC ATCATTCCTT CAACCCGTCC TGCAAATATC 240
CCACCTCTAC ATGCTAAAGG GAGACCCCTC ATGTTCCTTC CCCCAAACCC TGGCACTCCC 300
TTCTCCGGAT ATGTAGGTTG TCACCCCATA AACTACACAG TAGCTTCTCG CTTCTCGGCC 360
CTTAACGAGC TACTTACTAA CTTTAAAAGC CCCACAGAAA TGAACTTAAC TTGCAGGTCC 420
TCCACCTCCA CACTTGGCCC TGGGCGCCAT TCCTCTGAAA ATAATAGTAC CAACCCTTAC 480
AAAGACTCTG CCCATGCCCC ACTGTCACCA ACGAATTCCT TTTCCAGAAG GAAAAGGAAA 540
CAGGTTCTTC AGGCTCCTCT TCCAACCTCT TCACCAGTGA CTCCCCTCCA AGGTTCGTGG 600
ACTCTACCCC CGCAGTTTTC CTCCCCTCAC TCCCGGGCCT CTGCCCACCT CACCAACTCT 660
CCCTGCGCTC CCTGTCCCAG AGCCAAGCGG CGGCCGCTCC ACTCTCCCAA CTTAGAAGTT 720
CTGCCTCTAT CACCTGTTCT CACTAGAGCT TCCTCTCAGC CCAGCGGCCC ACCTTTGCCC 780
TGGCCTGCCT CTCTCCACCC CTTCGAGTCC TCCTGCCCAG GAAACACCCC CACGAGTCAG 840
TTCCGGGGTG CCTGTCGGAT TCAACTTCCC ATCCGTGGGA TTCCCACCCC CGGGGTCATG 900
CTCCCCTTCT CCATCACCTG CTCCGCCCAT AGCCAGATGA CATCCGCCGC TGCCTCCTCC 960
TCCATTCCCC TTCTCGGACG CCAGGTCCCC GGCCACTCAC CGCCCTCCGT GCGCGCCAGC 1020
CGCCCCCTCC GGTGGGGAAG AGGGGGGCGT GCACCCCAAC CCGCGCCCCC CCCCCACGAC 1080
ACGCACCTGT TCTTCCTCCT CTTCCCCTCG GCGGGCCGCG CCGGCGCCCC GACCCCCACC 1140
CTTGCCGCCT CCCGGCCTCC CGGAGCCCCG 1170
|
