Variant report

Variant	rs4635494
Chromosome Location	chr2:181727706-181727707
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]
rs10930943	0.96[CEU][hapmap];0.81[CHB][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10930944	0.96[CEU][hapmap];0.81[CHB][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12618669	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12624291	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12693262	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12995535	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3923258	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4128869	0.93[JPT][hapmap]
rs4267479	0.96[CEU][hapmap];0.81[CHB][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4283381	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4315481	0.93[JPT][hapmap]
rs4346342	0.92[ASN][1000 genomes]
rs62178176	0.81[ASN][1000 genomes]
rs6724902	0.92[JPT][hapmap]
rs7575713	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7588156	0.83[AMR][1000 genomes]
rs7590308	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:181727600-181728400	Enhancers	HUES48 Cell Line	embryonic stem cell

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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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