| Tag | Content |
|---|
EnhancerAtlas ID | HS062-11301 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr3:53147520-53148630 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:53148114-53148133 | CTACCACTAGGGGGCACTG | + | 7.88 |
|
| | 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 |
| GH03I053112 | chr3 | 53146746 | 53149190 |
|
Enhancer Sequence | ACCTGTCTCA GTCATGTGGG CCCCTGTTCT GGGCAGAAAG CCCATCCGTG AAGAGCAATG 60
CTATCCAGTA GAAATGTAAT GTTAAATTTT CTAGCAGCCA CAGTGCACAG GAAAAAGAAA 120
CAAGTGAAAT TAATTTTAAT ATATTTTATT TAACCAAAAT ATTATCATTT CAACAAGTAA 180
TCCCTGTAAA AAATATTTTT TTTCATATTA AGACTTTGAA ATCCAATATG TATTTTGCAT 240
TTATGACTCA TCTGAATTCA GACTAGCCAT ATTCCAGAAT GCTCTATAGC CACATGTGGC 300
TGGTGGCTAA CATTTGGGAC AGGGCAAGCC TAGAGCACCT CTGAAAGCAA GGATCACTTC 360
TAGCCCCCAT TCTCTTTACT CCTTGGTTTC TGAGCCTTTT TTCCAGACAC AGGGAGTGCA 420
AGTGTGAATC CTCCCAAACA GTGCAGCCCT CAGGGAATCA GAGAACCTAG AGCAGATGCC 480
AGGTTATCTC TTTAGCCCAG GAGTAAATCT TCCCTGATGA GAAGGAAATT GGGCCACAAG 540
ATGTTTAAAA CAGGCCATCT CCTTTCCCCG GAACAAAGAG CACCAGACAA CTTCCTACCA 600
CTAGGGGGCA CTGGGGACCA CGTCATCTTC AGACTTGGAT TCTGACCACA GCCGGCTTCA 660
GCACCTTCTC TCTCTCACAC TGCTCCTCAC CCCTTGCCAT GCTGTGGTGG TCCTCCCAGG 720
GGTCAGCAAA GCAGGACCTG TCCCCTTTTA AAAGGAAACG AAGGCTGCTG CTTGTCATGA 780
GGCTCTCGTG ATGCCTGTTT GCCTGCAGGT TGTGAATGGA TTTGGGAAGA TGATTGAGCT 840
CTTTAAAGAC AAAGTTCTTT GGGAGAATGA GATCATGATG GTGTACCTAA TCTGAGAGCT 900
CATACTTGAT TTTCCTAATG CCTTTGGTTT AAATGGGCCT GTGGTTCAGA AGGAATGGTG 960
ACACCACTTA CTAAAAGTGC TCATTAAGGA CACAGAGGCA GGAAATCCAA TCTGAGATGC 1020
GGCTTCTGCA GGCAGGGGCT GAGTGGTGGG AGAGAGGAAG CATATGGTGG ACTGTTACCA 1080
TTCTATTCAG AATGGAGGTT CAGAATGGAG 1110
|
