Variant report

Variant	rs57359242
Chromosome Location	chr18:30057483-30057484
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1035799	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10502601	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11664267	0.93[ASN][1000 genomes]
rs1458864	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1458867	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17744057	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17744336	0.93[ASN][1000 genomes]
rs2172388	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72639476	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72639477	0.87[AMR][1000 genomes];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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