Variant report

Variant	rs209811
Chromosome Location	chr6:11963797-11963798
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12193434	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16872098	0.86[EUR][1000 genomes]
rs169716	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs209799	0.80[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs209808	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6939106	0.86[JPT][hapmap]
rs7775818	0.87[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.92[EUR][1000 genomes]
rs9349041	0.91[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11961200-11966200	Enhancers	K562	blood
2	chr6:11961400-11972600	Weak transcription	Lung	lung
3	chr6:11963600-11964200	Enhancers	Fetal Intestine Small	intestine
4	chr6:11963600-11966600	Enhancers	Fetal Intestine Large	intestine

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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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