| Tag | Content |
|---|
EnhancerAtlas ID | HS176-10661 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr12:121340580-121341640 |
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 | CAGGTCCCCC ACTCCTACGA TCATGCCATT TCTTGCTTCC TCACTCTCCA GCTATGACTT 60
CCTTCTCACT ACCCGATTTC CACTCTTCAT GGATACTGCC ATCATTCCTT CAACCCGTCC 120
TGCAAATATC CCACCTCTAC ATGCTAAAGG GAGACCCCTC ATGTTCCTTC CCCCAAACCC 180
TGGCACTCCC TTCTCCGGAT ATGTAGGTTG TCACCCCATA AACTACACAG TAGCTTCTCG 240
CTTCTCGGCC CTTAACGAGC TACTTACTAA CTTTAAAAGC CCCACAGAAA TGAACTTAAC 300
TTGCAGGTCC TCCACCTCCA CACTTGGCCC TGGGCGCCAT TCCTCTGAAA ATAATAGTAC 360
CAACCCTTAC AAAGACTCTG CCCATGCCCC ACTGTCACCA ACGAATTCCT TTTCCAGAAG 420
GAAAAGGAAA CAGGTTCTTC AGGCTCCTCT TCCAACCTCT TCACCAGTGA CTCCCCTCCA 480
AGGTTCGTGG ACTCTACCCC CGCAGTTTTC CTCCCCTCAC TCCCGGGCCT CTGCCCACCT 540
CACCAACTCT CCCTGCGCTC CCTGTCCCAG AGCCAAGCGG CGGCCGCTCC ACTCTCCCAA 600
CTTAGAAGTT CTGCCTCTAT CACCTGTTCT CACTAGAGCT TCCTCTCAGC CCAGCGGCCC 660
ACCTTTGCCC TGGCCTGCCT CTCTCCACCC CTTCGAGTCC TCCTGCCCAG GAAACACCCC 720
CACGAGTCAG TTCCGGGGTG CCTGTCGGAT TCAACTTCCC ATCCGTGGGA TTCCCACCCC 780
CGGGGTCATG CTCCCCTTCT CCATCACCTG CTCCGCCCAT AGCCAGATGA CATCCGCCGC 840
TGCCTCCTCC TCCATTCCCC TTCTCGGACG CCAGGTCCCC GGCCACTCAC CGCCCTCCGT 900
GCGCGCCAGC CGCCCCCTCC GGTGGGGAAG AGGGGGGCGT GCACCCCAAC CCGCGCCCCC 960
CCCCCACGAC ACGCACCTGT TCTTCCTCCT CTTCCCCTCG GCGGGCCGCG CCGGCGCCCC 1020
GACCCCCACC CTTGCCGCCT CCCGGCCTCC CGGAGCCCCG 1060
|
