Variant report

Variant	rs16872108
Chromosome Location	chr6:11956092-11956093
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs16872077	0.82[CEU][hapmap];1.00[JPT][hapmap]
rs16872098	0.91[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs17533974	0.82[CEU][hapmap];1.00[JPT][hapmap]
rs209778	1.00[JPT][hapmap]
rs6919575	0.85[ASN][1000 genomes]
rs6928723	0.89[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7775818	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs9296224	0.85[ASN][1000 genomes]
rs9296237	1.00[JPT][hapmap]
rs9357253	0.81[ASN][1000 genomes]
rs9366941	0.81[ASN][1000 genomes]
rs9380630	0.82[CEU][hapmap];1.00[JPT][hapmap]
rs9380639	0.83[AMR][1000 genomes]
rs9380705	0.85[ASN][1000 genomes]
rs9380706	0.85[ASN][1000 genomes]
rs9394442	0.88[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs9394473	1.00[JPT][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11955400-11958800	Weak transcription	K562	blood

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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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