| Tag | Content |
|---|
EnhancerAtlas ID | HS060-28695 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr5:176886270-176887430 |
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 | chr5:176886670-176886691 | GGAGGAGGAGGAAGAGGAGGA | + | 11.13 | | ZNF263 | MA0528.1 | chr5:176886673-176886694 | GGAGGAGGAAGAGGAGGAGGA | + | 11.79 | | ZNF263 | MA0528.1 | chr5:176886679-176886700 | GGAAGAGGAGGAGGAGGAAGG | + | 8.17 | | ZNF263 | MA0528.1 | chr5:176886667-176886688 | AGGGGAGGAGGAGGAAGAGGA | + | 8.34 | | ZNF263 | MA0528.1 | chr5:176886676-176886697 | GGAGGAAGAGGAGGAGGAGGA | + | 9.83 | | Zfx | MA0146.2 | chr5:176886575-176886589 | CCCGCCGAGGCCTG | + | 7.22 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_68732 | chr5:176886798-176887622 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I177453 | chr5 | 176880440 | 176887291 |
|
Enhancer Sequence | TGTGGAACAA ACCCCAGGTG GGTCAGTGAG GGCGGGGGAG CCGGGTGAGA CAGGATTGTC 60
CACCTTGGGG CCTGGCCAGC ACCTCCTCTC TGGAATCTGG GTGGGGGCTG GGAGCTCTCC 120
AGCCCCACCA GGGGCCAGAC TACAGCTCCA GACCCTGTAA GCTAGGCCCC TGGAGGCCAG 180
TGCCCCATAA GGCCAGGGGC AAGAGGCAGG CAGTGCCTGC CCTGGGGGCA AACACCAGAG 240
ATCAGCGGTC AGACTGGGGG AGTGAGGGCG GGGGGCTGCT GGGAAGCGGG GCCCTCCTTA 300
CCACCCCCGC CGAGGCCTGG GGCTGCTACC TACATGGGAG GGAGGAAGAG AGGTTTGGGG 360
TGCGGTGGCA GGTGATATAG GGAAAGGGAG TCCGTGGAGG GGAGGAGGAG GAAGAGGAGG 420
AGGAGGAAGG CCCACTGTCC GATGCCTTTA TGAAAGGGCA GTACGGACGA CCTGCCGAGA 480
GAGACAGACA GAGAAAGAGA CAGAGGACAA GAGAGGGTCA GTCTCCCCCA CCCCTGCCCG 540
AGGCCTCTCC CGCCCCCAGG GCCTGGCCCT GGATGTCCAA GCTGCCTTCA GCCAGGGGCA 600
CAATCAGCCA AGCCAGCCGC AGCCTCACAC CAGCCCCAGA CACACAGCCA GCCTGGGAGC 660
AGTACAGCAG GGACGGCCTG TGGCGGGACC CCAGCATGGG GCAAGCACAC TCAGACCAGC 720
AGACAGGGCA GGGAAGAGCT TCAGGAGAGG CGGAAGCAGC ACACTGAGAA GCGGAACGGG 780
GACACCTGGG TGCAAGCTCC GGGAGGCTCC CTCAGGCCCG GGGCAAGAGC CCAGCACGCA 840
TGCATTCCGG CCTTCCAGGC CAGACCTAAT TCACCCCAGC CGAGCTGCTC CCCGTGGCCA 900
GCGCTGTGCC TCAGCCCATG CCAGAGCTGC CCCACAGGCC CTAGCACTCC CCACTGTTCA 960
GCCACAAGCG ACTTCACCAC CATCCCTGGC CCTTCTTGGG GTCCTGCCAC CTGGGAAGTG 1020
GTGGGCGGAT GCACGCTGGA TGAAGGGTCT CGCCTTCTCC AAGGGTTGCT TGGGCAAGGC 1080
CTCCCTTCTG AGAGAGTCCC AGAGAGGCTC AGGGCCGCAA CCTGAGGAGT GGGGCCGGAC 1140
GGGGGGTGGG GCCTAGGACT 1160
|
