Variant report

Variant	rs61826952
Chromosome Location	chr1:174637937-174637938
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10157872	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10158096	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10494493	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12063802	0.84[EUR][1000 genomes]
rs12563930	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12565810	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12568182	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16847257	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16847271	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16847402	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16847450	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1964103	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2072758	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34952844	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35216639	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs41524947	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56674178	0.86[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs57353443	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57366106	0.81[EUR][1000 genomes]
rs61439796	0.86[AFR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61826887	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61826888	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61826902	0.83[ASN][1000 genomes]
rs61826903	0.83[ASN][1000 genomes]
rs61826904	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61826909	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61826913	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61826917	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61826918	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61826921	0.88[ASN][1000 genomes]
rs61826923	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61826924	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61826925	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61826941	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61826942	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61826949	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61826950	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61826951	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61826953	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61826956	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61826957	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61826959	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61828062	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61828064	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61828065	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61828068	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61828081	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61828087	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61828088	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61828121	0.81[EUR][1000 genomes]
rs7523516	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[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	nsv1014637	chr1:174265631-174826765	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv535208	chr1:174265631-174826765	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1014753	chr1:174271770-174694838	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2755184	chr1:174388343-174970343	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
5	nsv534381	chr1:174468168-174656796	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv1803591	chr1:174594575-174642336	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs61826952	SERPINC1	cis	Muscle Skeletal	GTEx

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174607600-174677800	Weak transcription	Primary B cells from cord blood	blood
2	chr1:174612400-174638200	Weak transcription	Aorta	Aorta
3	chr1:174630000-174641600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:174636000-174638400	Weak transcription	Liver	Liver

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