Variant report

Variant	rs827107
Chromosome Location	chr3:158080769-158080770
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1095625	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1095631	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1095632	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1103981	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11915781	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1193519	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1435637	0.83[EUR][1000 genomes]
rs1520657	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1520662	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1520666	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1625612	0.96[EUR][1000 genomes]
rs1656360	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1656362	0.98[EUR][1000 genomes]
rs1656367	0.98[EUR][1000 genomes]
rs1656371	0.98[EUR][1000 genomes]
rs1714508	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1714510	0.98[EUR][1000 genomes]
rs1714512	0.93[EUR][1000 genomes]
rs1714513	0.90[EUR][1000 genomes]
rs1714517	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1714526	0.98[EUR][1000 genomes]
rs1724650	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1724725	1.00[ASN][1000 genomes]
rs1730038	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2956471	0.93[EUR][1000 genomes]
rs6441191	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6779266	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6788695	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6804180	1.00[ASN][1000 genomes]
rs698978	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73170371	0.92[EUR][1000 genomes]
rs7651712	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827103	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827105	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827115	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827116	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827117	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827119	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827133	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827138	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827152	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827182	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827183	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827189	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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
6	nsv1014381	chr3:158070451-158350118	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs827107	RSRC1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:158055200-158086000	Weak transcription	Left Ventricle	heart
2	chr3:158076200-158087000	Weak transcription	Aorta	Aorta
3	chr3:158078200-158081200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr3:158078600-158082800	Weak transcription	Fetal Intestine Small	intestine
5	chr3:158078600-158084600	Weak transcription	Duodenum Mucosa	Duodenum
6	chr3:158078800-158080800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr3:158079200-158083400	Weak transcription	Primary B cells from cord blood	blood
8	chr3:158079400-158081200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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