Variant report

Variant	rs4873602
Chromosome Location	chr8:52689122-52689123
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:89)

rs_ID	r²[population]
rs10086504	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes]
rs10092494	0.88[AMR][1000 genomes]
rs10096943	0.86[JPT][hapmap]
rs10097328	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10101163	0.86[LWK][hapmap]
rs10102568	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10104368	0.98[ASN][1000 genomes]
rs10110304	0.81[JPT][hapmap]
rs1022317	0.86[JPT][hapmap]
rs10504127	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10504128	0.86[JPT][hapmap]
rs10504132	1.00[CHB][hapmap];0.92[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs1059041	0.86[JPT][hapmap]
rs1078888	0.86[JPT][hapmap]
rs10958299	0.86[JPT][hapmap]
rs11775601	0.86[JPT][hapmap]
rs11777885	0.94[JPT][hapmap]
rs11784921	0.88[JPT][hapmap]
rs12115132	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12678479	0.86[JPT][hapmap]
rs13250860	0.86[JPT][hapmap]
rs13257067	0.86[JPT][hapmap]
rs13257291	0.86[JPT][hapmap]
rs13261243	0.86[JPT][hapmap]
rs13275235	0.86[JPT][hapmap]
rs13281179	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs1517305	0.86[JPT][hapmap]
rs16916800	0.94[ASN][1000 genomes]
rs16916878	0.93[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs16916903	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16919843	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2020431	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2395857	0.86[JPT][hapmap]
rs28635761	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28652885	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3763547	0.81[JPT][hapmap]
rs3824266	0.86[JPT][hapmap]
rs4242479	0.87[LWK][hapmap]
rs4259408	0.86[JPT][hapmap]
rs4294173	0.86[JPT][hapmap]
rs4324911	0.86[JPT][hapmap]
rs4330683	0.86[JPT][hapmap]
rs4361755	0.86[JPT][hapmap]
rs4570148	0.86[JPT][hapmap]
rs4584139	0.86[JPT][hapmap]
rs4587320	0.86[JPT][hapmap]
rs4596648	0.86[JPT][hapmap]
rs4612332	0.86[JPT][hapmap]
rs4618684	0.86[JPT][hapmap]
rs4634632	0.86[JPT][hapmap]
rs4873608	0.86[JPT][hapmap]
rs4873609	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4873613	0.86[JPT][hapmap]
rs5002416	0.82[JPT][hapmap]
rs56128832	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56394995	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs58408501	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58591247	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59344101	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7008057	0.86[JPT][hapmap]
rs7008721	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7010217	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7011046	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7013587	0.86[JPT][hapmap]
rs7014075	0.86[JPT][hapmap]
rs7017450	0.86[JPT][hapmap]
rs73590413	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73592226	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7460311	0.86[JPT][hapmap]
rs7463120	0.86[JPT][hapmap]
rs7464192	0.86[JPT][hapmap]
rs7465225	0.86[JPT][hapmap]
rs753540	0.86[JPT][hapmap]
rs7815751	0.88[AMR][1000 genomes]
rs7829408	0.86[JPT][hapmap]
rs7835028	1.00[CEU][hapmap]
rs7843530	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs882492	0.86[JPT][hapmap]
rs884580	0.86[JPT][hapmap]
rs925763	0.86[JPT][hapmap]
rs9298463	0.85[JPT][hapmap]
rs9298464	0.86[JPT][hapmap]
rs9298466	0.86[JPT][hapmap]
rs9298467	0.81[JPT][hapmap]
rs950687	0.86[JPT][hapmap]
rs9643465	0.82[LWK][hapmap]
rs9643466	0.86[JPT][hapmap]
rs9643792	0.86[JPT][hapmap]
rs9643793	0.86[JPT][hapmap]

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	nsv932026	chr8:51858658-52758574	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv817615	chr8:52252405-53023384	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1018429	chr8:52411443-52878946	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv1034856	chr8:52411443-52886765	Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv831316	chr8:52660353-52842928	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	nsv1023825	chr8:52668824-52716137	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:52684800-52691800	Weak transcription	Pancreas	Pancrea
2	chr8:52686000-52691800	Weak transcription	Right Atrium	heart
3	chr8:52686200-52691800	Weak transcription	Left Ventricle	heart
4	chr8:52686200-52703000	Weak transcription	Right Ventricle	heart

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