Variant report

Variant	rs9949349
Chromosome Location	chr18:30058198-30058199
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11081766	1.00[EUR][1000 genomes]
rs28360758	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28545765	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28584588	1.00[EUR][1000 genomes]
rs7242846	1.00[EUR][1000 genomes]
rs73421974	1.00[EUR][1000 genomes]
rs8086485	1.00[EUR][1000 genomes]
rs8097937	1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs9948201	1.00[EUR][1000 genomes]
rs9951044	1.00[EUR][1000 genomes]
rs9963014	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9963404	1.00[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30052000-30060000	Weak transcription	Fetal Intestine Small	intestine
2	chr18:30056800-30058400	Weak transcription	Fetal Brain Male	brain

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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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