Variant report

Variant	rs62481562
Chromosome Location	chr7:102839885-102839886
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs13224269	0.85[ASN][1000 genomes]
rs13229230	0.85[ASN][1000 genomes]
rs13229368	0.85[ASN][1000 genomes]
rs13237057	0.85[ASN][1000 genomes]
rs17136078	0.85[ASN][1000 genomes]
rs17136079	0.82[ASN][1000 genomes]
rs17606134	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1861731	0.85[ASN][1000 genomes]
rs1968200	0.85[ASN][1000 genomes]
rs1968201	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1968203	0.85[ASN][1000 genomes]
rs1968204	0.85[ASN][1000 genomes]
rs3987913	0.82[ASN][1000 genomes]
rs3987937	0.85[ASN][1000 genomes]
rs4266582	0.82[ASN][1000 genomes]
rs4336542	0.82[ASN][1000 genomes]
rs4360229	0.85[ASN][1000 genomes]
rs4428604	0.85[ASN][1000 genomes]
rs4480047	0.85[ASN][1000 genomes]
rs4523183	0.85[ASN][1000 genomes]
rs4727563	0.82[ASN][1000 genomes]
rs4729885	0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4729886	0.85[ASN][1000 genomes]
rs4729887	0.82[ASN][1000 genomes]
rs4729889	0.82[ASN][1000 genomes]
rs4729890	0.82[ASN][1000 genomes]
rs4729891	0.82[ASN][1000 genomes]
rs5025411	0.85[ASN][1000 genomes]
rs56711496	0.85[ASN][1000 genomes]
rs57125388	0.85[ASN][1000 genomes]
rs58962103	0.85[ASN][1000 genomes]
rs61581136	0.85[ASN][1000 genomes]
rs61591042	0.85[ASN][1000 genomes]
rs62480085	0.83[ASN][1000 genomes]
rs62480090	0.85[ASN][1000 genomes]
rs62480132	0.82[ASN][1000 genomes]
rs62480133	0.82[ASN][1000 genomes]
rs62480134	0.82[ASN][1000 genomes]
rs62481564	0.85[ASN][1000 genomes]
rs62481612	0.85[ASN][1000 genomes]
rs62481613	0.85[ASN][1000 genomes]
rs62481615	0.81[ASN][1000 genomes]
rs62481648	0.85[ASN][1000 genomes]
rs62484774	0.88[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs62484781	0.85[ASN][1000 genomes]
rs62484782	0.85[ASN][1000 genomes]
rs62484783	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62484784	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7804020	0.81[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	nsv868996	chr7:102332827-102991361	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv831084	chr7:102778908-102964970	Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	esv1794417	chr7:102814101-102928545	Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1031395	chr7:102816661-102868998	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
5	nsv970567	chr7:102833853-102850992	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs62481562	RP11-401L13.5	cis	Thyroid	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102839600-102840400	Enhancers	K562	blood

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