Variant report

Variant	rs1965558
Chromosome Location	chr7:64321367-64321368
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 40 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10258594	0.82[CEU][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10271473	0.83[EUR][1000 genomes]
rs11769995	0.81[EUR][1000 genomes]
rs11773228	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11773456	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12532791	0.81[EUR][1000 genomes]
rs13223142	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13225933	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13236444	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13236784	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1830007	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1966140	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2017252	0.92[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34238742	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35058955	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35065007	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3813700	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3829003	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4644117	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4717222	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4718156	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4718169	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4718170	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56063644	0.86[EUR][1000 genomes]
rs62455121	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62458435	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6460199	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs6460209	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6946377	0.81[EUR][1000 genomes]
rs6953002	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6957266	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6960979	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6980403	0.81[EUR][1000 genomes]
rs7776640	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7777724	0.81[EUR][1000 genomes]
rs7782713	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7796024	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7796284	0.92[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7797115	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7798063	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7798465	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7804955	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs7805817	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7810293	0.88[CEU][hapmap];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7810539	0.82[CEU][hapmap]
rs7811163	0.81[EUR][1000 genomes]
rs867630	0.81[EUR][1000 genomes]
rs9638209	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422405	chr7:63709739-64632341	Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
2	nsv427787	chr7:63741770-64419520	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	esv2755057	chr7:63819849-64345822	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
4	nsv464518	chr7:63881238-64506904	Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv607312	chr7:63881238-64506904	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
6	nsv888274	chr7:63990100-64331123	Strong transcription ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
7	nsv888275	chr7:63990100-64468590	Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv888276	chr7:63990100-64511564	Strong transcription ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv888279	chr7:64094285-64331123	Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
10	nsv1022042	chr7:64226499-64566945	Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
11	nsv1026390	chr7:64240323-64414364	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
12	nsv1033291	chr7:64273434-64406276	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
13	nsv508457	chr7:64286522-64391112	Strong transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
14	esv1797468	chr7:64296309-64356050	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	nsv888282	chr7:64299645-64511564	Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
16	nsv1018967	chr7:64318129-64380869	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:40)

SNP	Gene	Cis/trans	Tissue	Source
rs1965558	RP11-797H7.3	cis	lung	GTEx
rs1965558	RP11-460N20.5	cis	Nerve Tibial	GTEx
rs1965558	ZNF273	cis	Thyroid	GTEx
rs1965558	RP11-797H7.3	cis	Adipose Subcutaneous	GTEx
rs1965558	RP11-460N20.5	cis	Artery Tibial	GTEx
rs1965558	SEPHS1P1	cis	Thyroid	GTEx
rs1965558	RP11-797H7.3	cis	Whole Blood	GTEx
rs1965558	RP11-797H7.3	cis	Stomach	GTEx
rs1965558	RP11-797H7.3	cis	Heart Left Ventricle	GTEx
rs1965558	RP11-797H7.5	cis	lung	GTEx
rs1965558	RP11-460N20.5	cis	Adipose Subcutaneous	GTEx
rs1965558	ZNF273	cis	lung	GTEx
rs1965558	RP11-460N20.5	cis	Thyroid	GTEx
rs1965558	SEPHS1P1	cis	Nerve Tibial	GTEx
rs1965558	RP11-797H7.3	cis	Thyroid	GTEx
rs1965558	RP11-460N20.5	cis	Whole Blood	GTEx
rs1965558	RP11-797H7.3	cis	Nerve Tibial	GTEx
rs1965558	SEPHS1P1	cis	Skin Sun Exposed Lower leg	GTEx
rs1965558	SEPHS1P1	cis	Muscle Skeletal	GTEx
rs1965558	ERV3	cis	multi-tissue	Pritchard
rs1965558	RP11-797H7.5	cis	Adipose Subcutaneous	GTEx
rs1965558	RP11-797H7.3	cis	Artery Aorta	GTEx
rs1965558	SEPHS1P1	cis	Artery Tibial	GTEx
rs1965558	RP11-797H7.5	cis	Stomach	GTEx
rs1965558	RP11-797H7.5	cis	Skin Sun Exposed Lower leg	GTEx
rs1965558	RP11-797H7.3	cis	Esophagus Mucosa	GTEx
rs1965558	RP11-797H7.3	cis	Artery Tibial	GTEx
rs1965558	RP11-460N20.5	cis	lung	GTEx
rs1965558	RP11-797H7.5	cis	Artery Tibial	GTEx
rs1965558	RP11-797H7.3	cis	Esophagus Muscularis	GTEx
rs1965558	RP11-797H7.5	cis	Heart Left Ventricle	GTEx
rs1965558	SEPHS1P1	cis	Esophagus Muscularis	GTEx
rs1965558	CCT6P3	cis	Skin Sun Exposed Lower leg	GTEx
rs1965558	RP11-460N20.4	cis	Adipose Subcutaneous	GTEx
rs1965558	INTS4L1	cis	Skin Sun Exposed Lower leg	GTEx
rs1965558	ZNF273	cis	Heart Left Ventricle	GTEx
rs1965558	RP11-797H7.5	cis	Thyroid	GTEx
rs1965558	RP11-797H7.5	cis	Nerve Tibial	GTEx
rs1965558	RP11-797H7.3	cis	Muscle Skeletal	GTEx
rs1965558	RP11-797H7.3	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:0 , 50 per page) page:

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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