| Tag | Content |
|---|
EnhancerAtlas ID | HS060-04994 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr11:198590-199360 | 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 | chr11:198878-198899 | GAAAGAAGAGGAGGAGGAAAA | + | 6.18 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCCACCCCA ACTGAGAACA GAGAATCACC CCCAACCATC TGAACCCTCC CCCGGAACCC 60
AGGACCCACC AGTTCGGCCC TGCCTTGCCA ATGCCCCTCA GCCCCCTCAG CCCTTCACCC 120
TCTGGGCACC TGCCACGTGC TGGGGTTACA CTGCAGTGGT GAGGAGGGGC AGGCAACAGG 180
CCAGAAGGGA GACGCCCTGG CCCCAGCATG GACCGTGCTG AGGACAAGAG ATGGGGTTTA 240
GGAAGCACTG TCTGGAGAGA GAGAGGCAAT CTTAGATAGG GTAGCATGGA AAGAAGAGGA 300
GGAGGAAAAA ATAAACCATG AGCTATTTGG GGGAGGAGGG TCCTGGTTTC AGAAACAGCC 360
AGTGCAAAGC CCCTGGGTGG CACATGCCTG AGAGCTTGAG GGGCCTGAGA TGGGGAAGCA 420
GCATCATGGC ACCCAACAGC CCTCGTCCAT GTTGATTTTG CCAGCCCCAG GCCCTCAGGT 480
CCAACAGGGC AGCAACAGCC TCTCTCACAC ACGCTCAGCG ATGTTCCCAG GACTGGCACA 540
CACTGGGGAT GCCATTGCCA GCGTGAGGCT GAAATGGAGG AAGTGACCCC CACATGAGGT 600
ACCCCACAAG CAGTGGGGTG TGATCTCCAC AGTGTGACAG AAGACAGAAG GGGACCTTGA 660
TGCACGGGCA CCAACTTGTA GCTGACCCTG TTGACTCAGA GCCTGAGTTT GCTCCCTGTC 720
CTCTAGGGCC ACACGCCCTG GGTAGGCCGA GTTGGTCTGA GCCTCCTTTA 770
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