Variant report

Variant	rs11157261
Chromosome Location	chr14:42497648-42497649
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1471852	0.89[EUR][1000 genomes]
rs1684683	0.89[EUR][1000 genomes]
rs1684706	0.87[EUR][1000 genomes]
rs1684715	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1684719	0.88[EUR][1000 genomes]
rs1763277	0.89[EUR][1000 genomes]
rs1763279	0.88[EUR][1000 genomes]
rs1763281	0.89[EUR][1000 genomes]
rs1763282	0.89[EUR][1000 genomes]
rs1763283	0.89[EUR][1000 genomes]
rs2029184	0.89[EUR][1000 genomes]
rs923208	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv564563	chr14:42477256-42644617	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42497200-42499000	Enhancers	Primary B cells from cord blood	blood
2	chr14:42497600-42497800	Enhancers	Placenta Amnion	Placenta Amnion

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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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