Variant report

Variant	rs12361867
Chromosome Location	chr11:105323624-105323625
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10750721	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10895815	0.80[AMR][1000 genomes]
rs10895823	0.92[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10895830	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12806606	0.84[ASN][1000 genomes]
rs1375428	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1945960	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1945977	0.88[AFR][1000 genomes]
rs2084509	0.87[ASN][1000 genomes]
rs2409097	0.85[ASN][1000 genomes]
rs35935092	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7924758	0.89[AFR][1000 genomes]
rs7935262	0.89[AFR][1000 genomes]
rs7936610	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7938098	0.89[AFR][1000 genomes]
rs9988917	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949337	chr11:104950007-105510193	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv556221	chr11:105243371-105392079	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105316200-105327600	Weak transcription	K562	blood

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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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