Variant report

Variant	rs9815951
Chromosome Location	chr3:79371968-79371969
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11918897	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs12629799	0.83[YRI][hapmap]
rs13084055	1.00[CHB][hapmap]
rs1563382	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17016815	1.00[ASN][1000 genomes]
rs1809208	1.00[ASN][1000 genomes]
rs1869801	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs324755	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[YRI][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs324756	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4533610	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[YRI][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6802032	1.00[ASN][1000 genomes]
rs73109179	0.88[EUR][1000 genomes]
rs7429701	1.00[CHB][hapmap]
rs7622444	1.00[CHB][hapmap]
rs7637338	1.00[CHB][hapmap]
rs9809987	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9813399	1.00[ASN][1000 genomes]
rs9845808	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[YRI][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2763281	chr3:79246361-79489765	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv460727	chr3:79264611-79406519	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv590736	chr3:79264611-79406519	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv460730	chr3:79286801-79411014	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv590737	chr3:79286801-79411014	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:79370400-79372600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:79370800-79373600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr3:79371000-79373800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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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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