Variant report

Variant	rs6694226
Chromosome Location	chr1:213539531-213539532
allele	A/G
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]
rs10746441	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1107412	0.99[EUR][1000 genomes]
rs11120115	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11120116	0.80[ASN][1000 genomes]
rs11120117	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1187783	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1187784	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1211362	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1875765	0.99[EUR][1000 genomes]
rs2033595	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2033597	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2359700	0.88[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4655360	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs965779	0.99[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213539000-213540800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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

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