| Tag | Content |
|---|
EnhancerAtlas ID | HS069-05858 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr3:53147320-53148800 |
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: 2 | Chromosome | Start | End |
| chr3 | 53147431 | 53147628 | | chr3 | 53147764 | 53148603 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I053112 | chr3 | 53146746 | 53149190 |
|
Enhancer Sequence | ATGCCTGGTT GATGTTAGGT TCTTAATCCT AGGGTACTTG CATTTTGAAA AGTAGTGATT 60
ATCCAAAGTG ATTACTTCTC AATGGTAGGA TTTCAGAGGG CTTTTTGGGA GGGGAGGGCT 120
GAATTACAAA GGCCAAGCCC ACTCTACCTC TCCAAAAGGT CAGCCACAGC TCTGGAAGTG 180
GGCCCAAGGG CAGGCCTGGA ACCTGTCTCA GTCATGTGGG CCCCTGTTCT GGGCAGAAAG 240
CCCATCCGTG AAGAGCAATG CTATCCAGTA GAAATGTAAT GTTAAATTTT CTAGCAGCCA 300
CAGTGCACAG GAAAAAGAAA CAAGTGAAAT TAATTTTAAT ATATTTTATT TAACCAAAAT 360
ATTATCATTT CAACAAGTAA TCCCTGTAAA AAATATTTTT TTTCATATTA AGACTTTGAA 420
ATCCAATATG TATTTTGCAT TTATGACTCA TCTGAATTCA GACTAGCCAT ATTCCAGAAT 480
GCTCTATAGC CACATGTGGC TGGTGGCTAA CATTTGGGAC AGGGCAAGCC TAGAGCACCT 540
CTGAAAGCAA GGATCACTTC TAGCCCCCAT TCTCTTTACT CCTTGGTTTC TGAGCCTTTT 600
TTCCAGACAC AGGGAGTGCA AGTGTGAATC CTCCCAAACA GTGCAGCCCT CAGGGAATCA 660
GAGAACCTAG AGCAGATGCC AGGTTATCTC TTTAGCCCAG GAGTAAATCT TCCCTGATGA 720
GAAGGAAATT GGGCCACAAG ATGTTTAAAA CAGGCCATCT CCTTTCCCCG GAACAAAGAG 780
CACCAGACAA CTTCCTACCA CTAGGGGGCA CTGGGGACCA CGTCATCTTC AGACTTGGAT 840
TCTGACCACA GCCGGCTTCA GCACCTTCTC TCTCTCACAC TGCTCCTCAC CCCTTGCCAT 900
GCTGTGGTGG TCCTCCCAGG GGTCAGCAAA GCAGGACCTG TCCCCTTTTA AAAGGAAACG 960
AAGGCTGCTG CTTGTCATGA GGCTCTCGTG ATGCCTGTTT GCCTGCAGGT TGTGAATGGA 1020
TTTGGGAAGA TGATTGAGCT CTTTAAAGAC AAAGTTCTTT GGGAGAATGA GATCATGATG 1080
GTGTACCTAA TCTGAGAGCT CATACTTGAT TTTCCTAATG CCTTTGGTTT AAATGGGCCT 1140
GTGGTTCAGA AGGAATGGTG ACACCACTTA CTAAAAGTGC TCATTAAGGA CACAGAGGCA 1200
GGAAATCCAA TCTGAGATGC GGCTTCTGCA GGCAGGGGCT GAGTGGTGGG AGAGAGGAAG 1260
CATATGGTGG ACTGTTACCA TTCTATTCAG AATGGAGGTT CAGAATGGAG GTGTCACTTG 1320
GGGCGGTCAA AAGAGGCCTA TTTCACAATA GCTGGGTTGG TACTGATGAG CTGATCTAAA 1380
TAGCCAGGAA TTTCCCTGGA ATACCCTGAC CAACAAGCCA TTCCACTGCC CTCACTGTAC 1440
TAACGGAGAA ATGGCGGCTA AGGTGGTAAA AGGTGATGGA 1480
|
