| Tag | Content |
|---|
EnhancerAtlas ID | HS041-04215 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr11:77740930-77742710 |
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 | chr11:77741939-77741960 | CTCTTCCCCTCCCTCTGCTCC | - | 6.38 |
|
| | 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 |
| GH11I078029 | chr11 | 77741041 | 77743350 |
|
Enhancer Sequence | CATTCTCCTG CCTCAGCCTC CCAAGTAGCT GGGACTACAG GCGCCCACCA CCACGCCTGG 60
CTAATTTTTT TTGTATTTTT TAGTAGAGAC AGGGTTTCAC CGTGTTAGCC AGGATGGTCT 120
CGATCTCCTG ACCTCATGAT CCACCTGCCT CAGCCTCCCA AAGTGCTGGG ATTACAGGTG 180
TGAGCCATCG CGCCTGGCCT TTCTGTGAGA AAATTTCTTT AGAGCAAGAG CTCTCTCTGT 240
CTCCATTCCT GGACAGGAAT ATAAAACCTG CTTGCTTCTT TTTTCCCCCC CTCCAATTGC 300
ATGTTCTTTC TTTGCCACCA ATGCAAAGTA GGAAAAAAAC TCAGTTTTCC AGTGACATTA 360
GCACATTTGA CCCTGGCAGT TCAAAATAGG CATTAGCACC TCCATTTTCT ATATGAGGAC 420
CCCAAGGCTC CCAGAGATGA AGCACCTCTT TGAGTCAGTC AGACCAGGAG ACGAGAGAGC 480
AGGGCTCTAG TTTCGGCTCT GCCACCAGTT TGCAGTACCA CCTTAGACAC GTCCCTGCCC 540
CTCTCTGGGC CTCAGTTCTC CACCTGTAAT ATGGTGGGGG TTTGTGTATT TTCTGAGATG 600
GTCTCTGTGA TCCTGCCTTG CTTGATGCTA TGGCAACAAA AGAATTCAAA CAGCCCCTTG 660
CTATTGCCTA TCACTGGATC TTGTTTCCCT TTGGCCTGAC TCCAAGAGCA AGCACTGCTT 720
CCTTCTGCCC TCCCCTCACT CACTCCCCTC TGTTCTTCAG GAGACAATGC GGCCAGCCCC 780
TCTCCCCTCC AGGCGGCTGG GCTTTAGGCC AGCCAGCCAA ATGGCAGCTG GGACTCAGAT 840
GAAAGGGCCC TCAGAAGGCT GCTTGTGGCA GAGTGCCCAG CCTAGCCCAG CCCAGGCTTG 900
GCAGCCTGGG GCTCAGCTGT GCCACGAGGC ATCCTGTCCA CCCGCTCCCA TACAAGGCTC 960
CCTCTGTGAG TCCTGCAGAG AAGGAGACCC CTGCCAACCC ACAAGGACCC TCTTCCCCTC 1020
CCTCTGCTCC ATACCTGCTT GAGAAATATG CAAGTCTGTA GAGAATGGTC CAGGACTACA 1080
TCAGATTGAT CTGACTGTGC CAGGCACTTT GGAGAGCTTT ATCCCATTGA CTCTTCAGAA 1140
TAACGCTGAT AGCAAGTAAT GGTTTTTTTT TTTTTTTTTT TGAGACAGAA TCTCACTCTG 1200
TCACCCAGAC TCTAGGCTGG AGTGCAGTGT CACTAACATA GCTAACTGAA GACTCGACAT 1260
CCTGGAATCA AGCAACCCTC CTGCCTTAGC CTCCCAAGTA GCTGGGATTA CCGCTAACAC 1320
CCAGCTAATT TTTTTTACTT TTTTGTAGAG ATGGTGTCTC ACTATGTTGC CCAGACTGGT 1380
CTCAAACCCC TGAGCTCAAG CAATCTTTCT ACCTTGGCCT CCCAAAGTAC TGAGATTACA 1440
GGTGTGAGCC ACCATACCTG CAATCTCTTT TTATTTATTT GTTTATTTTT TAAAATTTAT 1500
TTTATTTTTT TTGAGACAGG GTCTTGCTCT GTTGCCCAGG CTGCAGTGCA GTGGTGTGAT 1560
CTCGGCTCAC TGCAACCTCC GCCTCCAGAG TTCAAGCAAT TCTCCTGCCT CAGCCTCTCG 1620
AGTAGCTGGG ATTATAGGCA CCAGCCATCA TGCCTGGCTA ATTTTTGTAT TTTTTTTTTT 1680
TTTAGTAGAG ATGGGGTTTC ACCATGTTGG CCAGGTTGGT CTCAAACTCC TGATCTCTAG 1740
CGGTCTGCCC ACCTCGGCCT CTCAAAGTGC TGGGATTATA 1780
|
