| Tag | Content |
|---|
EnhancerAtlas ID | HS068-01730 |
Organism | Homo sapiens |
Tissue/cell | GM18526 |
Coordinate | chr14:95051280-95053620 |
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 | chr14:95053461-95053482 | ACCTCCTCTCCCTCCTTCCTC | - | 6.24 | | ZNF263 | MA0528.1 | chr14:95053462-95053483 | CCTCCTCTCCCTCCTTCCTCT | - | 6.24 | | ZNF263 | MA0528.1 | chr14:95053458-95053479 | TGCACCTCCTCTCCCTCCTTC | - | 6.84 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 95051288 | 95051671 | | chr14 | 95053234 | 95053306 |
|
Enhancer Sequence | CATGGTGGGA ACAGGTAGGG AGTGTCAGTG GGGGGAAGCC CAGACTCTGC TCACTCATTA 60
TCTGCAGATT AGGGCTATTG TTGGTGGCTA CTAAGTCAGG GATTTCAAAA TCAGGAAGAT 120
GCAGCCAGGA AAAGAGGAGG CAGGACTCTG CAGAGGAGGC AGGACTCTGC AGAGTCAGAG 180
TGATAACCGA GTCTGAGTCC AAGCTTTGCC AGTGTTAGCA AGCGACTCCA TCTCTCTGAA 240
CCTCGGATTA CCCATCTGTA AAATAGAGCT AGCAGCAAGA TGTACCTTTT TGGGTGGTGC 300
AGGGCTGAAG GAGTTGGCAC AGTGCCTGAA AGAGGGTGCG GGCAATGCGC CCAACTGCTG 360
TGGCTGCTGG GTTTGGTGCC AGGTTCGATT CTGCAGGCAG AAACTTCTAC ATGAGGCTCC 420
TTCTCGGAAG GAGCTCAGGA CACAATTTGG AGGCTGGGCT GGCAAGGGTG ACCTGCTGGA 480
GCTATTCAAC TTCACTTAAA GACAGGCCTG CAGTCCAAGC CTGCCCAATT CCTGAGACCA 540
TTCTCTCTCC ACTGCTGAGC CCCACGGCCA CTCTGCAAGG GATTTCCCAC CCACCTGTTT 600
GGGGCCCTTT GGAGTTTGGT TTTAATTGGG TCACGGGATG CTGTGACAGG CTGCCCCTGC 660
CTGGTGGGGA TCTGGGGTCA CTGATGACAT TGTGCCCATG GAGAGAGCCC AGCAGAAAGG 720
GATTCCCTCC AAGGCGACAC ACAGGGCAAA GCTCACATCA GAAGCCAGGC AGGCCCTCTG 780
CACCTGGTAA TTAGCCAGCC TGGGTGCTGT CAGGCTCACA CGTGTGTGTG TGTGTGTGTG 840
TGTGTGTGTG TGTGTGTGTG TAAAGCATGT ACCCTATGGT ACAGTTGAGA ATATGGAGGC 900
CTCAGATGGG GCTTTTGCCA GAAACTGCCA TGCCTACTGC TCACACTTCC ATAGCACGTG 960
CCCCCAAGCA CCCCATGGTG TAGGTGCTGT TATTATCACT ATCTTACAGT TATGGAGCAG 1020
TGGCTCAAGG TGTAACTGAC TTGCCCAAAA TCACACTACA AGGACACAGC AGGGCTGAGA 1080
TTTGAACCCA GGCAGTGGCT TCAGAGCCTG AGCTGTTTCC TACTGCAGAG GGAGGAGGCA 1140
AGACTTCTAC CCGTAGCCAG ATGGGGAGGC ATGGGCACAG GAACGGCTCT TGGGTGAAGT 1200
GGAGGGAGGA AGAGGAGGAC TGAAGGCCAA GGCCACGTCA GGAGTGATGG GAGACCCCAC 1260
AAAGGCCTCC CTGAGAAGAG CTAGAGACAA AGATGAGTGC CTCCTCATCT GGAAGATGAA 1320
AAGATGTCTT TGCCTGCATG GGCTGCTGTC ACAAAGTCCC AGGGGCTAGG GGGCTTCAAC 1380
AACAGAAATT TCTTTCTTTA CAACTCTGGA AGCTGGAAGT CTGAGATTAA GGCACCAGCA 1440
GGATTTGTTC CTTCCAAGGC CCCTCTCCTT GGCTCACAGG TGGCTGCCTT CTCCCTGTCT 1500
TCACCTGGTC TTCCCTCTGT GCATGTCTCT ATCCTGATCT CCTCTTTTTA ATTTTTGTGT 1560
AAGGACGTAG TCATATTGGG TTGGGGCCCA CTCTAGTGAC CTCATTCTAA CTCAGTCCCC 1620
TCTTTAAAAG CCCTATCTCC AGATATAGTC ACATTCTGGG GTATTGAAGG TAAGGACTTC 1680
AGCATATGCA TTTTGGGGGC ACAATTCAGC CAGAACAGGA GGACGGTGGG GATGTCCACA 1740
TGAAGAGGTT CAGGCAGAAT TCCTTTAGGA GGGGAAGATG TCTCTCTGTG GGACAAGGGT 1800
GGCATGGAGC AGCCCCTGGG GGAAGGAGAA GGGGACAGTT TGCATACTGG TATTCTGCCT 1860
ACCCCAGGGT GGACACTCAC TCAGCGTTTG CTGAATGAAC AGGGCAAGGC CAGCAGTGCT 1920
GATGGTCCCA GGCATGTAGC TGGTCTGAGT TCATAGAAGG ACCACAGCGC CCTGCCATGT 1980
GCCAAACCAG GACACCAGAG TGAAGGCCAG AAGCTCACAT GGAAGCAGCT TAGTTCCCTG 2040
GTAACCTCGA GATGCTGATG AGACAGAGCA GAGCAGAGGG AACCCTCTCC CTCCATATCC 2100
CATCCTCCAA AATGTGTCCC TTGATGTGGA TGGGTAGACA GGATTCCTGC CCTGGCAGCC 2160
AGACCCCTGC CTTGGGTCTG CACCTCCTCT CCCTCCTTCC TCTCCCCGTC ATCCCTAAAT 2220
CTTGTCCTCG AGCCACTGCC ACCCTGTGTA AACCCTCATG CCCAGTCTTG CGGGTGCCAT 2280
CCCTTCTCTT TGAAGCTGAA TGGACCAAAC ATACCCATTG AGTGTTGGGT GGGGACATCT 2340
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