Variant report

Variant	rs17636197
Chromosome Location	chr4:21083087-21083088
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 95 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10014546	0.81[ASN][1000 genomes]
rs10022535	0.94[CHB][hapmap];0.91[CHD][hapmap];0.81[GIH][hapmap];0.94[JPT][hapmap];0.81[MEX][hapmap];0.91[TSI][hapmap];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10032561	0.88[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap]
rs10433822	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10516374	0.82[JPT][hapmap]
rs10938827	0.82[CHD][hapmap];0.88[JPT][hapmap]
rs10938831	0.82[ASN][1000 genomes]
rs10938837	0.82[JPT][hapmap]
rs11735843	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11735844	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11736507	0.85[AFR][1000 genomes];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11736572	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11935122	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11944165	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11945600	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap]
rs11945646	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap]
rs11945692	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap]
rs12233886	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12510687	0.81[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap]
rs12639638	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12640310	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12640491	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs12642886	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12644882	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12644941	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12646316	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12647437	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1364832	0.82[JPT][hapmap]
rs1364833	0.82[JPT][hapmap]
rs1364838	0.82[JPT][hapmap]
rs1364839	0.82[JPT][hapmap]
rs1368646	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1368648	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17446667	0.82[JPT][hapmap]
rs17447922	0.82[JPT][hapmap]
rs17447985	0.82[JPT][hapmap]
rs17448106	0.82[JPT][hapmap]
rs17448392	0.82[JPT][hapmap]
rs17506080	0.82[JPT][hapmap];0.89[MEX][hapmap]
rs17506108	0.82[JPT][hapmap]
rs17513252	0.82[JPT][hapmap];0.86[MEX][hapmap]
rs17574283	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17637027	0.86[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];0.88[CHD][hapmap];0.87[GIH][hapmap];1.00[MEX][hapmap];0.82[TSI][hapmap];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2043387	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2043388	0.81[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];0.92[GIH][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs2113966	0.82[JPT][hapmap];0.89[MEX][hapmap]
rs2163931	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2163933	1.00[CEU][hapmap];0.82[CHB][hapmap];0.88[CHD][hapmap];0.87[GIH][hapmap];0.82[JPT][hapmap];0.90[MEX][hapmap];0.82[TSI][hapmap]
rs2163934	0.88[CHB][hapmap];0.94[JPT][hapmap]
rs28406534	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2874892	0.82[JPT][hapmap]
rs4572877	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4574407	1.00[CEU][hapmap];0.94[CHB][hapmap];0.91[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap]
rs4590029	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4599408	0.94[CHB][hapmap];0.94[CHD][hapmap];0.94[JPT][hapmap];0.91[TSI][hapmap];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4615170	1.00[CEU][hapmap];0.93[CHB][hapmap];0.94[JPT][hapmap]
rs55737345	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55885656	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55957496	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs56025335	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56139613	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56412118	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58548088	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59223154	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59416831	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60444813	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61644618	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6810466	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6810897	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6815915	0.92[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6817687	0.93[CEU][hapmap];0.94[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.97[TSI][hapmap];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6832569	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6832607	1.00[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6835991	0.82[JPT][hapmap]
rs6840528	0.94[CHB][hapmap];0.94[CHD][hapmap];0.81[GIH][hapmap];0.94[JPT][hapmap];0.81[MEX][hapmap];0.91[TSI][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6845231	0.81[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];0.81[GIH][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs6854888	0.86[CHB][hapmap];0.94[JPT][hapmap]
rs6855710	0.94[CHB][hapmap];0.94[JPT][hapmap]
rs6858766	1.00[CEU][hapmap];0.94[CHB][hapmap];0.91[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap]
rs720852	1.00[CEU][hapmap];0.82[CHB][hapmap];0.88[JPT][hapmap]
rs720853	1.00[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap]
rs73802481	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7658908	0.82[ASN][1000 genomes]
rs9997060	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014941	chr4:20611726-21345226	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537053	chr4:20611726-21345226	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv829878	chr4:20966047-21138626	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv878745	chr4:21054348-21155716	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv878746	chr4:21054348-21169062	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv878747	chr4:21057794-21169062	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3467025	chr4:21080942-21086055	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3467026	chr4:21080942-21086055	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv17854	chr4:21081080-21086557	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv2760912	chr4:21082551-21085342	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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