Variant report

Variant	rs4852844
Chromosome Location	chr2:72280792-72280793
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11902394	0.92[ASN][1000 genomes]
rs11902497	0.92[ASN][1000 genomes]
rs13406776	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1400681	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1400682	0.90[AMR][1000 genomes]
rs17007725	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17007727	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17665497	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17722207	1.00[CHB][hapmap];0.92[ASN][1000 genomes]
rs4852841	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4852847	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4852852	0.92[ASN][1000 genomes]
rs56808687	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59496509	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72904426	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72904430	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72904452	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:72278800-72280800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr2:72278800-72281000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr2:72280600-72281000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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