Variant report

Variant	rs7012499
Chromosome Location	chr8:34351136-34351137
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10099045	0.99[ASN][1000 genomes]
rs10100459	0.99[ASN][1000 genomes]
rs12375320	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12546239	0.82[ASN][1000 genomes]
rs12547877	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12678112	0.82[ASN][1000 genomes]
rs16882264	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16882360	0.94[EUR][1000 genomes]
rs16882460	0.80[AMR][1000 genomes]
rs2028776	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28366982	0.94[EUR][1000 genomes]
rs28503648	0.97[ASN][1000 genomes]
rs28545279	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4739366	0.87[AMR][1000 genomes]
rs4739565	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55752257	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55849895	0.82[ASN][1000 genomes]
rs56036407	0.80[AMR][1000 genomes]
rs56091526	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs56355533	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs59516528	0.90[ASN][1000 genomes]
rs6468262	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6993906	0.82[ASN][1000 genomes]
rs72640929	0.90[AMR][1000 genomes]
rs72640930	0.83[AMR][1000 genomes]
rs72640938	0.87[AMR][1000 genomes]
rs7464162	0.90[ASN][1000 genomes]
rs7815684	0.82[ASN][1000 genomes]
rs7816886	0.94[ASN][1000 genomes]
rs7827467	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7834257	0.94[ASN][1000 genomes]
rs7836137	0.94[ASN][1000 genomes]
rs953272	0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv6147	chr8:34314029-34359124	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34350600-34351400	Enhancers	Fetal Heart	heart
2	chr8:34351000-34351800	Enhancers	Fetal Kidney	kidney

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