Variant report

Variant	rs4610631
Chromosome Location	chr7:19109966-19109967
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10224508	1.00[EUR][1000 genomes]
rs10227338	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10227439	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10228000	0.80[AMR][1000 genomes]
rs10229075	1.00[EUR][1000 genomes]
rs10240640	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10244882	0.96[EUR][1000 genomes]
rs10251015	1.00[EUR][1000 genomes]
rs10252615	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10256776	1.00[EUR][1000 genomes]
rs10265255	0.96[EUR][1000 genomes]
rs10266725	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10268126	0.80[AMR][1000 genomes]
rs10270859	1.00[EUR][1000 genomes]
rs10275030	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10275229	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11981706	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11981966	0.80[AMR][1000 genomes]
rs1548576	1.00[EUR][1000 genomes]
rs17140565	1.00[ASN][1000 genomes]
rs17423728	1.00[ASN][1000 genomes]
rs2078978	1.00[EUR][1000 genomes]
rs2214627	1.00[EUR][1000 genomes]
rs2263233	1.00[EUR][1000 genomes]
rs2521720	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2521722	1.00[EUR][1000 genomes]
rs2521723	0.87[EUR][1000 genomes]
rs2521734	1.00[EUR][1000 genomes]
rs2521735	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2521737	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2717337	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2717340	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2717361	0.93[EUR][1000 genomes]
rs2717362	1.00[EUR][1000 genomes]
rs2717364	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2717365	1.00[EUR][1000 genomes]
rs28579949	1.00[ASN][1000 genomes]
rs28611415	1.00[EUR][1000 genomes]
rs28627595	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28720702	1.00[ASN][1000 genomes]
rs2892913	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2905456	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2905459	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2906045	0.96[EUR][1000 genomes]
rs2965021	0.96[EUR][1000 genomes]
rs2965030	1.00[EUR][1000 genomes]
rs429	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4383884	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60301616	1.00[EUR][1000 genomes]
rs60744788	1.00[EUR][1000 genomes]
rs6953130	1.00[EUR][1000 genomes]
rs6960648	1.00[ASN][1000 genomes]
rs6964820	1.00[ASN][1000 genomes]
rs6965235	1.00[ASN][1000 genomes]
rs6971603	0.96[EUR][1000 genomes]
rs6972974	0.80[AMR][1000 genomes]
rs6973803	1.00[EUR][1000 genomes]
rs73314876	1.00[EUR][1000 genomes]
rs73323561	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7776577	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs886227	1.00[EUR][1000 genomes]
rs9655162	1.00[EUR][1000 genomes]
rs975893	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531020	chr7:18971153-19261019	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1032503	chr7:19092460-19134995	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1032126	chr7:19092460-19137228	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	esv2761116	chr7:19092472-19136307	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv532096	chr7:19094324-19361216	Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv519024	chr7:19103926-19134119	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv532097	chr7:19105767-19302951	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19102600-19118000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:19106600-19111400	Weak transcription	NHDF-Ad	bronchial
3	chr7:19106800-19118600	Weak transcription	Muscle Satellite Cultured Cells	--

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