Variant report

Variant	rs62466312
Chromosome Location	chr7:101337751-101337752
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10239715	1.00[ASN][1000 genomes]
rs10269590	1.00[ASN][1000 genomes]
rs10270145	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10278430	0.88[AMR][1000 genomes]
rs10278534	1.00[ASN][1000 genomes]
rs10447812	1.00[ASN][1000 genomes]
rs11771998	0.92[AMR][1000 genomes]
rs11772618	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12667267	1.00[ASN][1000 genomes]
rs1619382	1.00[ASN][1000 genomes]
rs1636440	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1636441	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1636442	0.89[AMR][1000 genomes]
rs1636443	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1636447	0.86[AMR][1000 genomes]
rs1722218	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1722224	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1722226	1.00[ASN][1000 genomes]
rs1722229	1.00[ASN][1000 genomes]
rs2529183	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28650269	0.91[AFR][1000 genomes]
rs4263675	1.00[ASN][1000 genomes]
rs4276617	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4436052	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4490765	1.00[ASN][1000 genomes]
rs4535653	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4602818	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4642556	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4727503	1.00[ASN][1000 genomes]
rs4727504	1.00[ASN][1000 genomes]
rs4727505	1.00[ASN][1000 genomes]
rs4727506	1.00[ASN][1000 genomes]
rs4729747	1.00[ASN][1000 genomes]
rs56381219	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60702821	0.88[AMR][1000 genomes]
rs62463667	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs62463668	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs62463669	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs62463670	0.85[AMR][1000 genomes]
rs62463671	0.88[AMR][1000 genomes]
rs62463672	0.92[AMR][1000 genomes]
rs62463674	0.92[AMR][1000 genomes]
rs62463675	0.88[AMR][1000 genomes]
rs62463676	0.92[AMR][1000 genomes]
rs62463677	0.88[AMR][1000 genomes]
rs62466309	1.00[ASN][1000 genomes]
rs62466310	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62466343	1.00[ASN][1000 genomes]
rs62466344	1.00[ASN][1000 genomes]
rs62466345	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466346	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466347	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466348	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466349	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466350	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62466351	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466354	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466355	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466356	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466357	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62466358	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467460	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467463	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467464	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467465	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467466	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467468	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467469	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6957219	1.00[ASN][1000 genomes]
rs6960571	1.00[ASN][1000 genomes]
rs757820	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs757821	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs757822	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs757823	1.00[ASN][1000 genomes]
rs757824	1.00[ASN][1000 genomes]
rs7785622	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799319	1.00[ASN][1000 genomes]
rs7809926	1.00[ASN][1000 genomes]
rs7811421	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs848644	1.00[ASN][1000 genomes]
rs848645	1.00[ASN][1000 genomes]
rs848646	1.00[ASN][1000 genomes]
rs848654	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	nsv933653	chr7:100701931-101515782	Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv1018544	chr7:101225639-101424889	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv539045	chr7:101225639-101424889	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh 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
4	nsv482758	chr7:101231458-101395219	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv831079	chr7:101273495-101466776	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101332000-101376800	Weak transcription	Right Atrium	heart
2	chr7:101335800-101339600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:101337400-101338000	Enhancers	HepG2	liver
4	chr7:101337400-101342800	Weak transcription	Rectal Mucosa Donor 31	rectum

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