Variant report

Variant	rs28627595
Chromosome Location	chr7:19101799-19101800
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10216193	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10227338	1.00[ASN][1000 genomes]
rs10227439	1.00[ASN][1000 genomes]
rs10228000	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10229095	1.00[EUR][1000 genomes]
rs10235982	0.92[EUR][1000 genomes]
rs10240640	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10248134	0.92[EUR][1000 genomes]
rs10248747	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10249481	1.00[EUR][1000 genomes]
rs10251141	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10251600	0.92[EUR][1000 genomes]
rs10252615	1.00[ASN][1000 genomes]
rs10253091	1.00[EUR][1000 genomes]
rs10256989	1.00[EUR][1000 genomes]
rs10263856	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10266725	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10268126	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10268428	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10270625	1.00[EUR][1000 genomes]
rs10274013	1.00[EUR][1000 genomes]
rs10275030	1.00[ASN][1000 genomes]
rs10275229	1.00[ASN][1000 genomes]
rs10279195	1.00[EUR][1000 genomes]
rs10279917	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11971269	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11974081	1.00[EUR][1000 genomes]
rs11974849	1.00[EUR][1000 genomes]
rs11975276	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11975863	1.00[EUR][1000 genomes]
rs11976041	1.00[EUR][1000 genomes]
rs11980713	1.00[EUR][1000 genomes]
rs11981268	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11981706	1.00[ASN][1000 genomes]
rs11981966	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17140565	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17140629	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17423728	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2521720	1.00[ASN][1000 genomes]
rs2521735	1.00[ASN][1000 genomes]
rs2521737	1.00[ASN][1000 genomes]
rs2717337	1.00[ASN][1000 genomes]
rs2717340	1.00[ASN][1000 genomes]
rs2717364	1.00[ASN][1000 genomes]
rs28399914	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28572026	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28579949	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28720702	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28753114	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28797565	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28803198	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28820332	1.00[EUR][1000 genomes]
rs2892913	1.00[ASN][1000 genomes]
rs2892914	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2905456	1.00[ASN][1000 genomes]
rs2905459	1.00[ASN][1000 genomes]
rs429	1.00[ASN][1000 genomes]
rs4383884	1.00[ASN][1000 genomes]
rs4610631	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60781112	1.00[EUR][1000 genomes]
rs6943143	1.00[EUR][1000 genomes]
rs6945718	1.00[EUR][1000 genomes]
rs6950144	1.00[EUR][1000 genomes]
rs6960648	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6964820	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6965235	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6970557	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6971116	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6972974	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73323561	1.00[ASN][1000 genomes]
rs7776577	1.00[ASN][1000 genomes]
rs975893	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19086200-19101800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:19101200-19102000	Weak transcription	HSMMtube	muscle
3	chr7:19101200-19102200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr7:19101200-19105400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr7:19101200-19105400	Weak transcription	HSMM	muscle
6	chr7:19101400-19102800	Enhancers	NHDF-Ad	bronchial
7	chr7:19101400-19105200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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