| Tag | Content |
|---|
EnhancerAtlas ID | HS127-02057 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr1:159906700-159907470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:159907433-159907454 | TCCTCCCCGTCCTTCTCCACC | - | 6.35 | | ZNF263 | MA0528.1 | chr1:159907204-159907225 | GAAGCAGGAGGGAAGAGAAAG | + | 6.3 | | ZNF263 | MA0528.1 | chr1:159907421-159907442 | TCCCCATCCTCCTCCTCCCCG | - | 6.49 | | ZNF263 | MA0528.1 | chr1:159907430-159907451 | TCCTCCTCCCCGTCCTTCTCC | - | 8.24 | | ZNF263 | MA0528.1 | chr1:159907427-159907448 | TCCTCCTCCTCCCCGTCCTTC | - | 8.36 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09609 | chr1:159906051-159909005 | CD14 | | SE_28185 | chr1:159905613-159916500 | Fetal_Intestine | | SE_29354 | chr1:159905717-159916603 | Fetal_Intestine_Large | | SE_52604 | chr1:159906346-159910513 | Small_Intestine | | SE_59359 | chr1:159879583-159907614 | Ly3 | | SE_63399 | chr1:159883649-159916570 | NCI-H69 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCAAGGGAGA CAGGCATCAG GGGCCCCAGT GGGGCTGTCA GCCCAAAAAG CAGTGTCCAA 60
GGGCCAGGGA GACCACTCAG GGCTCCAGCC TGCTGCCCAC CCACCAGCCC TGCCTCATAG 120
GAGTCCTCAG CCCAGGGCCA CCCTGTCTAC TGCACCCAGG CCAAATGAGG ATTCTGTCAA 180
CCCACCCCCA CACACTGGCC TGGGGCTGAA CCCAGGTTGG ATGTCCAGAG CCTGGGGGAG 240
AGCCAAGCCC CCTCAGGAGG AGCACTGTTC TGGGAGTGAG GAGGCCTGGG TCCTAGACTC 300
TGCTCTGCCA CTAATCAGTG GCATGACTCA GCCTCACCTA TGCAATGGGA ATGATTATGA 360
CCTCCTTCCT ACTTAGGAGT GAGAGATAAA TAATAAGGGC TTGGGTGAAA AGGTATTTTG 420
AAAACACAAG GTGCTATATA TATGTGAGCT GTGTTTCACT CAGGGCCCAA GAGCCCCTCT 480
CTCCCACCCA CTTCCCTGGC CAGGGAAGCA GGAGGGAAGA GAAAGAGGGA GTTCCTGACA 540
CCGAGCCTAG AAGGCTGATT GAATTTATAT TTGAAGAACT GAAAAGGGCA GGAGTGTGGG 600
GGAGGGGTGA GATGCAACTA CTAAGTGAGC AAACAAGGGC TCTCAGGAAG GGTGGGGCAT 660
CAGAGCTGTT TGTGGGATGG AAATAGAACT CCCTCTTCCC CTTTCTCCCA CCAGCCAGAG 720
ATCCCCATCC TCCTCCTCCC CGTCCTTCTC CACCACCTGC CCCCCAGCTT 770
|
