| Tag | Content |
|---|
EnhancerAtlas ID | HS024-02238 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr10:134050690-134052360 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAX | MA0058.3 | chr10:134051020-134051030 | AGCACGTGGT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr10 | 134050730 | 134050822 | | chr10 | 134051065 | 134051145 | | chr10 | 134051357 | 134051749 | | chr10 | 134051926 | 134052169 |
|
Enhancer Sequence | CTGGACTGTG CTCCCTGGAC TGTGCTCCCT GGGCTCACAG GCTGGGCCCC TCTGCCCTCC 60
ACTGGCGTTT GCTCCTCCCA AGCCAGGTGA CCTGACCAGA GGCCAGTAGG GCCACCTCTC 120
TGGCCTCAGC TTCCTTGCAG CTCTAAGGCA AAGGCAAGGA CCATGCACAC GCCTGTCGAG 180
GGAAGAAAAT GAGAAAATGG ATATGAAAGT TCTCCTCCTC CTCCTGAATC AGTCATGAGG 240
GAAACAGCTA TTTTAAGGCA TAAAGGTGCA GCCTGGGTGA CCCAGAGAGA CGGGCCCGGC 300
AAATTCCCAC CGCCTTTTGG CCCATTTAGG AGCACGTGGT AACCACTCCT TCCTAAGCAG 360
ACTCTGCGCC GAGGTCCCCA CGCAGGGTTT CTTTGCTCCT GCAGTGGTGG CGGAGGTGAA 420
CCCAAAGCAG AGGGCGAGGC ACAGAGGAAC CTGAGTGTGC CGGCGGGGCT GGCCCCGGTG 480
CAGCTCCATC CCTCTGCCCC CAAGTGCAGC TTCACCCCTC TTCCCCCAAG TGTGTGCCGG 540
CGGGGCTGGC CCGGTGTGGC TTCACCCCTC TGCCCCTAGA GCCTGGAGGA GAACCAGCCC 600
TGGAAGAATC AGCTTCCCCA CAGCAGGGAG AGCAGGATCC CCCTTTCCCG ACCATTTAGG 660
AACCTCCAGC TGCCTTGTAC ACAGGGCTCC TCCGGGTTCT CTAATCAGTG CTGCCATCCC 720
CCTCCCAACG CTGGCCTGGT GGGAGGTGAT CTGTTTAATC CTCAGCATCT CTGCCTCCCT 780
CCAAAGCCAC TGTGGTCAGA CCCAGCACAG CCTGGAGCCC CCGAGACTCT CCAGCCCTGA 840
CCCTCCCAGA GAAAAGGCAG CTGCTAAGCT GGGCCCCTCA GTGTGGCAGG CAAGTGGACG 900
AGGCCTGGGG AACTGCCAGC AGTGCTGGCG GGGGAACTTC CTCCCACCAT CTGGCCAGGG 960
CACGGGGCAG CCTCCTTGGG ACCGAGGCAG CTTCTACTGA GGACTGTGGT GCAGCAGCTG 1020
CTCTCGGAGG CCCCCACGGG AAGCTACACA GCAGGTCCAA GAGATCCACA TGATTCAGGA 1080
GATGCCCCTT GCTTTAAAAT GTAGGTTTTA TTATCACACA GGTGGGTGAG ATCAGGAGAT 1140
GCCTGCCATT GATGAGACCG TTCGTTATAG TTACCAACAG GAGGAGGGGC ATGCCACACC 1200
GTGGGGCCAC ACAGCAAAGA CCAGGGTCTC GGAGGCAGAC GACGTGAAGG GGAAACACGG 1260
GCAGAGCCTT AGTGGAGGCT TCCTCGGGAA AAGCAGGGAA AGGCGGGGAA AGCCAGGTGA 1320
GCAGGTTTGA GACTGGCCTG TGGGAATACA GGCCTGCCCT GGTTGTCTGG GGTCAGGTCC 1380
TGAGGTGATT CATGCAGGGG ATGTGGGCTC AAGCCTGGGA AAGCATAGAG CAGACGGCTG 1440
GGGGTGAGCT GGGGGTTGCA TTTGAAAGGC AACCAAAGGC AAGTGTTTCT GATCTCTAGG 1500
AAGTGGCTGG CCCAGGAGGG GCAGTCTCTC CAGGGTCAGC AAGGCCCTGA CATTAAAGCG 1560
TTGGAAATAC ACAGTTCATA CATGTGCAAT GCATGCACAC ACACACACAT ACCACATACA 1620
CACATGCACA CACAGAGGCA TGCACACACA CGCAACACAC AGACATGCAG 1670
|
