Variant report

Variant	rs827119
Chromosome Location	chr3:158039582-158039583
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1095625	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1095631	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1095632	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1103981	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11915781	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1193519	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1435637	0.81[EUR][1000 genomes]
rs1520657	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1520662	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1520666	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1608099	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1625612	0.95[EUR][1000 genomes]
rs1656360	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1656362	0.96[EUR][1000 genomes]
rs1656367	0.96[EUR][1000 genomes]
rs1656371	0.96[EUR][1000 genomes]
rs1714508	0.96[EUR][1000 genomes]
rs1714510	0.96[EUR][1000 genomes]
rs1714512	0.91[EUR][1000 genomes]
rs1714513	0.88[EUR][1000 genomes]
rs1714517	0.96[EUR][1000 genomes]
rs1724650	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1724725	1.00[ASN][1000 genomes]
rs1730038	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2956471	0.91[EUR][1000 genomes]
rs4680416	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6441191	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6779266	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6788695	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6804180	1.00[ASN][1000 genomes]
rs698978	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73170371	0.90[EUR][1000 genomes]
rs7651712	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827103	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827105	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827107	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827115	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827116	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827117	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827133	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827138	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827152	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827182	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827183	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827189	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9845600	0.89[EUR][1000 genomes];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	nsv1013391	chr3:157505943-158115553	Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv536775	chr3:157505943-158115553	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1002378	chr3:157715428-158673414	Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv877689	chr3:157858930-158133307	Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv916910	chr3:157926799-158183372	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs827119	RSRC1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:157986400-158040000	Weak transcription	Primary B cells from cord blood	blood
2	chr3:157993400-158054600	Weak transcription	Primary T cells from cord blood	blood
3	chr3:157993800-158040600	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr3:158019200-158041600	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr3:158035600-158047400	Weak transcription	Left Ventricle	heart

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