| Tag | Content |
|---|
EnhancerAtlas ID | HS095-07935 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:121340600-121341640 |
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 | TCATGCCATT TCTTGCTTCC TCACTCTCCA GCTATGACTT CCTTCTCACT ACCCGATTTC 60
CACTCTTCAT GGATACTGCC ATCATTCCTT CAACCCGTCC TGCAAATATC CCACCTCTAC 120
ATGCTAAAGG GAGACCCCTC ATGTTCCTTC CCCCAAACCC TGGCACTCCC TTCTCCGGAT 180
ATGTAGGTTG TCACCCCATA AACTACACAG TAGCTTCTCG CTTCTCGGCC CTTAACGAGC 240
TACTTACTAA CTTTAAAAGC CCCACAGAAA TGAACTTAAC TTGCAGGTCC TCCACCTCCA 300
CACTTGGCCC TGGGCGCCAT TCCTCTGAAA ATAATAGTAC CAACCCTTAC AAAGACTCTG 360
CCCATGCCCC ACTGTCACCA ACGAATTCCT TTTCCAGAAG GAAAAGGAAA CAGGTTCTTC 420
AGGCTCCTCT TCCAACCTCT TCACCAGTGA CTCCCCTCCA AGGTTCGTGG ACTCTACCCC 480
CGCAGTTTTC CTCCCCTCAC TCCCGGGCCT CTGCCCACCT CACCAACTCT CCCTGCGCTC 540
CCTGTCCCAG AGCCAAGCGG CGGCCGCTCC ACTCTCCCAA CTTAGAAGTT CTGCCTCTAT 600
CACCTGTTCT CACTAGAGCT TCCTCTCAGC CCAGCGGCCC ACCTTTGCCC TGGCCTGCCT 660
CTCTCCACCC CTTCGAGTCC TCCTGCCCAG GAAACACCCC CACGAGTCAG TTCCGGGGTG 720
CCTGTCGGAT TCAACTTCCC ATCCGTGGGA TTCCCACCCC CGGGGTCATG CTCCCCTTCT 780
CCATCACCTG CTCCGCCCAT AGCCAGATGA CATCCGCCGC TGCCTCCTCC TCCATTCCCC 840
TTCTCGGACG CCAGGTCCCC GGCCACTCAC CGCCCTCCGT GCGCGCCAGC CGCCCCCTCC 900
GGTGGGGAAG AGGGGGGCGT GCACCCCAAC CCGCGCCCCC CCCCCACGAC ACGCACCTGT 960
TCTTCCTCCT CTTCCCCTCG GCGGGCCGCG CCGGCGCCCC GACCCCCACC CTTGCCGCCT 1020
CCCGGCCTCC CGGAGCCCCG 1040
|
