Variant report

Variant	rs4956257
Chromosome Location	chr4:107403444-107403445
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs13113961	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17355932	0.85[CEU][hapmap];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2049209	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2280631	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2691803	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3108142	0.87[ASN][1000 genomes]
rs3108144	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3108145	0.85[CEU][hapmap];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4413480	0.95[EUR][1000 genomes]
rs4484374	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4495119	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6819528	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6825451	0.90[EUR][1000 genomes]
rs6850696	0.88[EUR][1000 genomes]
rs7673683	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs940617	0.85[CEU][hapmap];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:107402000-107403600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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