Variant report

Variant	rs10918315
Chromosome Location	chr1:165908704-165908705
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10800171	0.81[AFR][1000 genomes]
rs11577887	1.00[ASN][1000 genomes]
rs12120390	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12124634	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12730968	1.00[ASN][1000 genomes]
rs13375130	1.00[ASN][1000 genomes]
rs16853627	1.00[ASN][1000 genomes]
rs16853832	1.00[ASN][1000 genomes]
rs1934272	1.00[ASN][1000 genomes]
rs1934273	1.00[ASN][1000 genomes]
rs1934274	1.00[ASN][1000 genomes]
rs2349104	0.82[EUR][1000 genomes]
rs34075422	1.00[ASN][1000 genomes]
rs35774572	1.00[ASN][1000 genomes]
rs61836675	1.00[ASN][1000 genomes]
rs6685404	1.00[ASN][1000 genomes]
rs6698004	1.00[ASN][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	nsv872509	chr1:165885147-165917109	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv520206	chr1:165903962-165913774	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island 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	chr1:165904400-165912000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:165906800-165910600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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