| Tag | Content |
|---|
EnhancerAtlas ID | HS034-15571 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr19:49240460-49241190 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr19:49241056-49241066 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr19:49241073-49241083 | GCCCCGCCCC | + | 6.02 | | NFIC | MA0161.2 | chr19:49240953-49240964 | TACTTGGCAGA | + | 6.62 | | SP2 | MA0516.2 | chr19:49241052-49241069 | ACAAGCCCCGCCCCACC | + | 6.08 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_29817 | chr19:49239566-49242174 | Fetal_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTGAATATAT TATCCCATTG AATCCTCACC TAGGATTTTA CTGAGATTAA CTGGCACAGA 60
ATGGGTTGGA ATTCAAACCC CAGTTCAAAG CCCATCAGTT GAATTGCTAC AACATTCTAT 120
CTCCCAAAAG GAAGCTCAGA TACAGAAAAG CGTTTAGAAG GCTCCCTGAG CAGACCCGTG 180
CTTTCAATGC GCCAGGCCCC ACCCCTGCCA GGCGCGGTCC ACCACCAGCT GTTTGACCAT 240
TGACTCTACC TTCTGTTCCA GGCCTTCCTT CGCCTCTACA GTGATATCTT CCTTCAGCCC 300
CTTCCTTTCC CATGTGATCC CACTTGGCAG CCAACCCAGC CTAAGGCCGT CTTATCCAAG 360
GCCGGCCCCT CAGCGGCTCC GCCCATCTTA GTCCCAGCAG GCCTGATCTA GGAACCTGTA 420
TTCACTCACT CTGCAGGTGT CGCCCCCTTC TATACTCCAC CCACATAGGC CCTGCTCAGT 480
AGCCACCTCA ACCTACTTGG CAGAGCTGCC TCCTACCACA GAGACCCATG CTCACCACAT 540
GCCACCACTC CTCGCGGGAC CCAACAGTTT TTGCCCCAGA CCACGCTTTT CCACAAGCCC 600
CGCCCCACCA CAGGCCCCGC CCCACAACAT GCCCCGCCCA TCTGCTCTGC ATCGCTCCCA 660
AGAACATTGT CCGTGCTTAC TCTTCCGGCT CCTAGGTCTC CAATTCCTTT TTCTTTTTCT 720
GGAGGACAGT 730
|
