Variant report

Variant	rs4951695
Chromosome Location	chr1:211142741-211142742
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs11119654	0.87[ASW][hapmap];0.85[LWK][hapmap];0.99[MKK][hapmap]
rs12042686	0.92[CEU][hapmap];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12406562	0.95[AFR][1000 genomes]
rs1501548	0.87[ASW][hapmap];0.85[LWK][hapmap];0.99[MKK][hapmap]
rs1501549	0.87[ASW][hapmap];0.85[LWK][hapmap];0.99[MKK][hapmap]
rs1501550	0.83[LWK][hapmap];0.93[MKK][hapmap]
rs1501557	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1777250	0.83[CHD][hapmap]
rs1875438	0.85[CHD][hapmap]
rs4951693	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4951694	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6540648	0.87[ASW][hapmap];0.85[MKK][hapmap]
rs7524268	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7526579	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.80[TSI][hapmap];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7551412	0.90[YRI][hapmap];0.84[AFR][1000 genomes]
rs7553997	1.00[YRI][hapmap];0.95[AFR][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	esv3437481	chr1:211139629-211143927	Weak transcription	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4951695	ELK4	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211123000-211152000	Weak transcription	HSMM	muscle

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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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