Variant report

Variant	rs2270059
Chromosome Location	chr15:92715946-92715947
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 3 )

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

rs_ID	r²[population]
rs1165	1.00[CEU][hapmap];0.83[GIH][hapmap];0.84[MEX][hapmap];0.98[TSI][hapmap];0.99[EUR][1000 genomes]
rs17696379	0.82[CHB][hapmap]
rs2240589	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.98[TSI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2270060	1.00[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap];0.86[YRI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2270061	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4777722	1.00[ASW][hapmap];0.88[GIH][hapmap];0.87[LWK][hapmap];0.86[MKK][hapmap];0.82[YRI][hapmap];0.89[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs4777725	0.91[CEU][hapmap];0.97[EUR][1000 genomes]
rs6496900	0.89[YRI][hapmap];0.87[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs7176191	0.82[CHB][hapmap]
rs748853	0.82[YRI][hapmap];0.84[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs748854	0.82[YRI][hapmap];0.86[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs758133	0.85[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs758134	0.84[YRI][hapmap]
rs758135	0.89[YRI][hapmap];0.87[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs8033384	0.82[CHB][hapmap]
rs886912	0.82[YRI][hapmap];0.85[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs886913	1.00[ASW][hapmap];0.83[GIH][hapmap];0.89[LWK][hapmap];0.88[MKK][hapmap];0.89[YRI][hapmap];0.87[AFR][1000 genomes];0.85[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	nsv948621	chr15:92688981-93158095	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1037878	chr15:92713130-92739827	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2270059	SLCO3A1	cis	multi-tissue	Pritchard
rs2270059	FURIN	cis	cerebellum	SCAN
rs2270059	GABARAPL3	cis	parietal	SCAN

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:92687600-92719400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr15:92708000-92718400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr15:92708200-92719000	Weak transcription	Lung	lung
4	chr15:92708600-92716000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr15:92711600-92727200	Weak transcription	Left Ventricle	heart
6	chr15:92712400-92716400	Weak transcription	Fetal Heart	heart
7	chr15:92713000-92717400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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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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