| Tag | Content |
|---|
EnhancerAtlas ID | HS051-18070 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr21:44846070-44846880 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr21:44846519-44846530 | CCACACCCTGC | + | 6.62 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_11196 | chr21:44843317-44848801 | CD20 | | SE_34640 | chr21:44836922-44847063 | HeLa | | SE_52671 | chr21:44845571-44847049 | Small_Intestine | | SE_58455 | chr21:44763901-44850830 | Ly1 | | SE_59568 | chr21:44816711-44859975 | Ly3 | | SE_62541 | chr21:44767678-44851140 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACCTGCGGGG CCGCACAGAG CTCAGAGCCC ACCAGCGCCC CCGCCGCCCG CGGTCGGCTC 60
CATCCGTGCC CGCGGAGCCC CCAGTCCCCA CGGGACGCAG GGACCTGCTC CCACGCCTGT 120
CGCCCCCACT CTATCCACGG GCCCCTCCAG CCCCGTGGGA GGTGTGGACC CGCCCCCGCC 180
GCCCGCTCCA CCCGGACCCC CGACCCTCTT GAGCCCCGCG GGGCGCACGG ACCCGCTCTC 240
ATAGAGGCCC CTGCCGCCCG AGTCCGGTTC CGTCCCGATC CCGGGACCCC CTGAGCCGGG 300
ATTCCACACT CGCCTCCCGC CGCCCGCTGT CGGTTCCGTC CCCACCCTCG ACCCCTTTAG 360
CACCTCTGGG CGCGGACCCG CTCCCACACC TGGCCCTGCC ACCCGAGGTC GGCTCGATCC 420
GGATCCCAGG ACCGTCCCCT GCCCCGCTCC CACACCCTGC CCCCGCCGCC CGCGATCCGT 480
CCGGTCCCCA CCCCCGACAT CCCAGGCACC TCGGGGATCG CGGACCCGCC CCCCACACCC 540
GGTATCTCCG CCCGCGGTCG GCTCCAACCT GACCCCCGGC TCCCCAGCCC CTGAGCCCCG 600
CGGACTCACT CCTACCCCGG CCCCCCAACA AAGGGGAGCC CGAGGGCGGC CAGGCCGCCA 660
ACCCCGCCCG CGAACCCCGC GCGCGCAAGG CCAGGGACCC TGCGCGGTGG CTGCAACCCC 720
GAGCCCCGGC CCGGCGCCCG CGCGGAGCCC CCACGGCGGC CACCTCCGCC CGCCCGGAGC 780
CCGCCGCTGC CGCCGCTGCC GCCGCTGCCG 810
|
