Variant report

Variant	rs3099277
Chromosome Location	chr6:166597468-166597469
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10428861	1.00[AMR][1000 genomes]
rs13209161	0.81[AFR][1000 genomes]
rs1610311	1.00[CHB][hapmap]
rs3099271	0.81[AFR][1000 genomes]
rs3099272	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3099273	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3099274	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3099275	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3099276	1.00[AFR][1000 genomes]
rs3099278	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3099313	0.81[AFR][1000 genomes]
rs3127351	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3127353	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3127354	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3127360	0.81[AFR][1000 genomes]
rs34188346	0.81[AFR][1000 genomes]
rs34651251	0.81[AFR][1000 genomes]
rs34732671	0.81[AFR][1000 genomes]
rs55987387	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57391649	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57545167	1.00[AMR][1000 genomes]
rs57772015	0.81[AFR][1000 genomes]
rs58812582	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59151797	1.00[AMR][1000 genomes]
rs60819315	1.00[AMR][1000 genomes]
rs61611265	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73787031	1.00[AMR][1000 genomes]
rs73787034	1.00[AMR][1000 genomes]
rs73787040	1.00[AMR][1000 genomes]
rs73787049	1.00[AMR][1000 genomes]
rs73787055	1.00[AMR][1000 genomes]
rs73787058	1.00[AMR][1000 genomes]
rs73787070	1.00[AMR][1000 genomes]
rs73787192	1.00[AMR][1000 genomes]
rs7449736	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166587800-166608400	Weak transcription	Pancreas	Pancrea

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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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