Variant report

Variant	rs6772010
Chromosome Location	chr3:68575675-68575676
allele	A/G
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:15)

rs_ID	r²[population]
rs10514723	0.80[YRI][hapmap]
rs11713541	0.93[YRI][hapmap]
rs17047573	1.00[TSI][hapmap]
rs17047586	1.00[TSI][hapmap]
rs17047626	1.00[TSI][hapmap]
rs17047742	1.00[TSI][hapmap]
rs17047774	0.87[LWK][hapmap];0.83[MKK][hapmap];0.89[YRI][hapmap]
rs17047788	0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs2202976	1.00[TSI][hapmap];0.88[YRI][hapmap]
rs4855488	1.00[YRI][hapmap]
rs56064707	1.00[EUR][1000 genomes]
rs6771965	1.00[GIH][hapmap];0.80[JPT][hapmap];0.82[LWK][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap]
rs6809703	0.84[YRI][hapmap]
rs73837656	1.00[EUR][1000 genomes]
rs907081	0.85[YRI][hapmap]

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	esv1832396	chr3:68478762-68641509	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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