Variant report

Variant	rs291471
Chromosome Location	chr2:191190180-191190181
allele	A/C
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:16)

rs_ID	r²[population]
rs10182490	0.83[JPT][hapmap]
rs1366676	0.90[GIH][hapmap];0.83[JPT][hapmap];0.85[TSI][hapmap]
rs1595997	0.81[GIH][hapmap];0.83[JPT][hapmap];0.85[TSI][hapmap]
rs16832425	1.00[MEX][hapmap]
rs16832573	0.90[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2067383	0.97[ASN][1000 genomes]
rs2582734	0.90[GIH][hapmap];0.83[JPT][hapmap];0.85[TSI][hapmap]
rs2582741	0.83[JPT][hapmap]
rs2582756	0.83[JPT][hapmap]
rs291406	0.90[GIH][hapmap];0.83[JPT][hapmap];0.85[TSI][hapmap]
rs291408	1.00[ASW][hapmap]
rs291416	0.90[GIH][hapmap];0.83[JPT][hapmap];0.85[TSI][hapmap]
rs291432	0.94[ASN][1000 genomes]
rs291465	0.82[CHB][hapmap];0.92[JPT][hapmap];0.80[ASN][1000 genomes]
rs291473	0.98[ASN][1000 genomes]
rs59924974	0.89[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:191186000-191194600	Weak transcription	K562	blood

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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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