Variant report

Variant	rs10157872
Chromosome Location	chr1:174550507-174550508
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs12563930	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs12564876	0.87[ASN][1000 genomes]
rs12564992	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12565430	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12565810	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12568182	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16847257	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16847271	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1964103	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2072758	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34952844	0.83[EUR][1000 genomes]
rs35216639	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs41524947	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56674178	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57353443	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61439796	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61826863	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs61826865	0.86[ASN][1000 genomes]
rs61826867	0.88[ASN][1000 genomes]
rs61826868	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61826869	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61826873	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs61826876	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61826877	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61826879	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61826881	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61826882	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61826883	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61826887	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61826888	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61826902	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61826903	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61826904	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61826909	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61826913	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61826917	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61826918	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61826921	0.96[ASN][1000 genomes]
rs61826923	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61826924	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61826925	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61826941	0.80[EUR][1000 genomes]
rs61826942	0.80[EUR][1000 genomes]
rs61826949	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61826950	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61826951	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61826952	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61826953	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61826956	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61826957	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61826959	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs61828062	0.82[EUR][1000 genomes]
rs61828068	0.80[EUR][1000 genomes]
rs61828081	0.80[EUR][1000 genomes]
rs61828645	0.87[ASN][1000 genomes]
rs61828653	0.88[ASN][1000 genomes]
rs61828654	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9970174	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 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	nsv872555	chr1:174343705-174565720	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	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
6	nsv1007667	chr1:174438778-174556953	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv999295	chr1:174457532-174596961	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	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
9	esv2757762	chr1:174469281-174569776	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv2758979	chr1:174469281-174569776	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv548196	chr1:174525135-174559121	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv947553	chr1:174548435-174554898	ZNF genes & repeats Weak transcription Enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10157872	SERPINC1	cis	Muscle Skeletal	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174545200-174555800	Weak transcription	Psoas Muscle	Psoas
2	chr1:174546000-174573000	Weak transcription	Left Ventricle	heart
3	chr1:174546200-174556800	Weak transcription	Primary B cells from cord blood	blood
4	chr1:174547200-174554400	Weak transcription	Primary T helper cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links