Variant report

Variant	rs1968543
Chromosome Location	chr4:103155520-103155521
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 108 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs10433893	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10433991	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11097768	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11725311	0.86[ASN][1000 genomes]
rs11733504	0.88[ASN][1000 genomes]
rs11733720	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11736058	0.86[ASN][1000 genomes]
rs13111744	0.86[ASN][1000 genomes]
rs13111958	0.84[ASN][1000 genomes]
rs13111982	0.84[ASN][1000 genomes]
rs13112133	0.86[ASN][1000 genomes]
rs13126885	0.86[ASN][1000 genomes]
rs1348024	0.81[ASN][1000 genomes]
rs149268	0.86[ASN][1000 genomes]
rs151370	0.86[ASN][1000 genomes]
rs151413	0.82[ASN][1000 genomes]
rs151414	0.83[ASN][1000 genomes]
rs151416	0.82[ASN][1000 genomes]
rs17032332	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17032357	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs182865	0.86[ASN][1000 genomes]
rs190178	0.86[ASN][1000 genomes]
rs192068	0.86[ASN][1000 genomes]
rs2119209	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2119210	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2119211	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2119213	0.86[ASN][1000 genomes]
rs2165265	0.88[ASN][1000 genomes]
rs34376460	0.86[ASN][1000 genomes]
rs34922141	0.84[ASN][1000 genomes]
rs35301460	0.84[ASN][1000 genomes]
rs35610681	0.86[ASN][1000 genomes]
rs35700174	0.84[ASN][1000 genomes]
rs366374	0.84[ASN][1000 genomes]
rs368845	0.86[ASN][1000 genomes]
rs373091	0.85[ASN][1000 genomes]
rs380768	0.86[ASN][1000 genomes]
rs384085	0.83[ASN][1000 genomes]
rs384460	0.82[ASN][1000 genomes]
rs386682	0.84[ASN][1000 genomes]
rs387839	0.86[ASN][1000 genomes]
rs394649	0.85[ASN][1000 genomes]
rs406749	0.86[ASN][1000 genomes]
rs406954	0.86[ASN][1000 genomes]
rs408364	0.86[ASN][1000 genomes]
rs413462	0.86[ASN][1000 genomes]
rs418348	0.86[ASN][1000 genomes]
rs420823	0.86[ASN][1000 genomes]
rs430589	0.86[ASN][1000 genomes]
rs431984	0.84[ASN][1000 genomes]
rs432186	0.82[ASN][1000 genomes]
rs438803	0.86[ASN][1000 genomes]
rs440507	0.83[ASN][1000 genomes]
rs444943	0.86[ASN][1000 genomes]
rs4476601	1.00[ASN][1000 genomes]
rs448181	0.86[ASN][1000 genomes]
rs451078	0.84[ASN][1000 genomes]
rs452385	0.86[ASN][1000 genomes]
rs4525979	0.86[ASN][1000 genomes]
rs455610	0.86[ASN][1000 genomes]
rs455741	0.85[ASN][1000 genomes]
rs456349	0.86[ASN][1000 genomes]
rs456521	0.84[ASN][1000 genomes]
rs456985	0.85[ASN][1000 genomes]
rs457490	0.86[ASN][1000 genomes]
rs457736	0.86[ASN][1000 genomes]
rs458201	0.86[ASN][1000 genomes]
rs458943	0.86[ASN][1000 genomes]
rs459159	0.86[ASN][1000 genomes]
rs459331	0.86[ASN][1000 genomes]
rs459559	0.84[ASN][1000 genomes]
rs460026	0.85[ASN][1000 genomes]
rs460610	0.86[ASN][1000 genomes]
rs460755	0.86[ASN][1000 genomes]
rs461902	0.86[ASN][1000 genomes]
rs4621433	0.86[ASN][1000 genomes]
rs462186	0.86[ASN][1000 genomes]
rs463542	0.80[ASN][1000 genomes]
rs463721	0.85[ASN][1000 genomes]
rs463772	0.86[ASN][1000 genomes]
rs4640675	0.86[ASN][1000 genomes]
rs465144	0.86[ASN][1000 genomes]
rs465176	0.84[ASN][1000 genomes]
rs467204	0.86[ASN][1000 genomes]
rs58321370	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs593576	0.86[ASN][1000 genomes]
rs62323488	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62323492	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62323541	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62327916	0.99[ASN][1000 genomes]
rs642663	0.82[ASN][1000 genomes]
rs643119	0.84[ASN][1000 genomes]
rs643645	0.86[ASN][1000 genomes]
rs657195	0.86[ASN][1000 genomes]
rs658953	0.86[ASN][1000 genomes]
rs659837	0.84[ASN][1000 genomes]
rs660502	0.86[ASN][1000 genomes]
rs660580	0.86[ASN][1000 genomes]
rs6825428	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs682916	0.86[ASN][1000 genomes]
rs6852794	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6855701	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs688499	0.86[ASN][1000 genomes]
rs9995079	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869164	chr4:102483189-103213842	Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv428447	chr4:103103730-103262107	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1008680	chr4:103153709-103206555	Strong transcription Weak transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv3400242	chr4:103154579-103157077	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103155000-103155800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
2	chr4:103155000-103156000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:103155400-103156000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell

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