Variant report

Variant	rs12506993
Chromosome Location	chr4:107395400-107395401
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11938517	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2866904	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2866905	0.89[EUR][1000 genomes]
rs3018056	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3108137	0.87[EUR][1000 genomes]
rs3108139	0.89[EUR][1000 genomes]
rs3108140	0.89[EUR][1000 genomes]
rs3108141	0.88[EUR][1000 genomes]
rs3108143	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3108148	0.86[EUR][1000 genomes]
rs3113244	0.88[EUR][1000 genomes]
rs4383690	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4413480	0.81[AFR][1000 genomes]
rs6825451	0.83[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:107395200-107395600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

Quick Search:

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

what's new

Quick links