| Tag | Content |
|---|
EnhancerAtlas ID | HS060-12761 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr16:28650760-28652370 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr16:28651176-28651189 | ATATGCAAATAAG | - | 6.57 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CACACATATA TATATATTTT TTTTTTTTTT TTTTTGAGAC AGAGTTTCAC TCTGTCCCCC 60
AGGCTGGAGT GCAATGGCAC AATCTTGGCT CACTGCAACC TCCGTCTCCC GGGTTCAAGC 120
AATTCCTCTG CCTCAGCCTC TGAGTAGCTG GGACTACAGG TGTGCACCAT CATGCCCAGC 180
TAATTTTTGT ATTCTTAGTA GAGATGGGGT TTCACCATAT TGGCCAGGCT CGTGTCAACT 240
CCTGACCTCG TGATCTGCCC ACCGTGGCCT CCCAAAGTGC TGGGACTATA GGTGTGAGCC 300
GCTACACCCC GTCCAAGATA AAATTATTTT AACAATATAC TATGAAGAGA AAAACACTGG 360
CTATGAAAGA ATATGCATAG TTTTACCCTG TTTAAAAATA AAGATTGAAA GAATACATAT 420
GCAAATAAGT TTACTTTTAT TTTTGGTAAC ACTTTACTGC ATTGTCTGAA TATTGACAAT 480
CAGTATGCAT CATGAAGCTA CATGGCTAAC ATTGTGTACT CACTGTGTGT GCCAGGCCCT 540
GGGTTCAATG CTCTACATGC ACTTATATTT CATTTAATTC TCTCTGCAAC CTGAGATGGT 600
ATAGCCACCT CATTTTACAG AGTTGAAACT GAGGCTCAGA GACTGAAAGT TAAGCCTGAG 660
GTTACAGTCA ATAAGAGGCA GAGCTGGAAC TGAAACCTAT GTGTGTCTGA CCACCAGTTC 720
ATGTTCTGAC GGCAGGCTAG TCTGCATCAC AGAGTGTGGG GTAGATGGTG CATGCCTGCT 780
AGGATGGGCT AGGTATCACT GTAGGTAAGA AACAGCCCCA AACGATGGAA ATGTACAAAA 840
TGTACACCAC TGAAGGCTCT TTTCCTGCCC ATGCTGCACA TCCTCCATGG CTCTCCTGTG 900
CCCTGTGCCC CACATGCCCT CATCCTGCCA CGAGAATAAA GGAGCAGCCT CCATATAGGA 960
GCTGTCAGTT GCTCCAAGAG ATGAAGGAGA GAGTGGCCAG TCTCAATGGC TCCCAACTCT 1020
TTTGCCTCGA GGTGACACGC TTCACTTCCA CTCACATCTC CTGGGTCAAA GCAAATCCCA 1080
TGGGTACATC CACTTTCAAG TGGCCCAGGA GAGAACCTGA AATACTTGGT GGACTCCATT 1140
AAGACCGTCA TATGGTGTCA GCCTGCATGG GAGACTGTGG AGGGGCAGAG GAAGAGAGTG 1200
GGGAACTGAT GGGAAATGAC AGGAGGACTA AGTCACCGCA GATTTGCTTT ATCTTCAGCC 1260
AGGTGGAGTT TGTCCCAGAG CTGCACAAAA TCATCACCAG CATGATTAAA CGGAGTAGAC 1320
TTCAGAAAAA GCAGTTTGGT CGAATGTAAT CAGCAGTGAA CTCAGAATCA ATTGAGTGAC 1380
ATTGAGTCAG TAAATCTCTG ACTGCCTCAG TTACCCCATA TGATAGTTTT GAGGATGGGA 1440
ACATTGAGAG AGTTGATTTG GAAGGATATC AAGAGTAAAA ATTCCAACAT TTTAGTTCCT 1500
TTAAGTTAAA TCCAGGCACT GTCTTTCCTG CAAGTCTCCT GTTCCTTTCA GATTGCACAG 1560
GTGAGAGTGC TCAGATTAGG GCTGGAGGTT GTAAACTATT GCTCCCACAC 1610
|
| |
|
|
|
