Variant report

Variant	rs13101042
Chromosome Location	chr3:85172364-85172365
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10433523	0.82[EUR][1000 genomes]
rs11127873	0.83[EUR][1000 genomes]
rs11127876	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11713170	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13059053	0.91[ASN][1000 genomes]
rs13061527	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13064817	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13078494	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13097560	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1545926	0.99[ASN][1000 genomes]
rs2171140	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2200464	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2220244	0.99[ASN][1000 genomes]
rs2326128	0.82[EUR][1000 genomes]
rs34201102	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4410457	0.83[EUR][1000 genomes]
rs62250629	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6549011	0.82[EUR][1000 genomes]
rs6549012	0.83[EUR][1000 genomes]
rs6549016	0.97[ASN][1000 genomes]
rs66500121	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6765011	0.83[EUR][1000 genomes]
rs6775464	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6775752	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6788656	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6790864	0.83[EUR][1000 genomes]
rs6791035	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6796256	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6796393	0.83[EUR][1000 genomes]
rs6798922	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7623714	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7636138	0.84[EUR][1000 genomes]
rs9284802	0.83[EUR][1000 genomes]
rs9309969	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9309970	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs959236	0.93[ASN][1000 genomes]
rs9814600	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9814835	0.83[EUR][1000 genomes]
rs9819278	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9820587	0.84[EUR][1000 genomes]
rs9839194	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9875381	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9883252	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002058	chr3:84757044-85389876	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv3419993	chr3:85030343-85663403	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv492289	chr3:85066623-85319147	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2753915	chr3:85071410-85624810	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
5	nsv877093	chr3:85101501-85194054	Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv590897	chr3:85122624-85187085	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv877094	chr3:85124697-85253981	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv590898	chr3:85158733-85243777	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv877095	chr3:85163167-85290434	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv877096	chr3:85163167-85366517	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv460747	chr3:85163167-85391672	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv590899	chr3:85163167-85391672	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv1001124	chr3:85167047-85309046	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85168400-85177600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:85169200-85198600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr3:85170800-85173000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr3:85172200-85173000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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