Variant report

Variant	rs10864210
Chromosome Location	chr1:216016851-216016852
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10082095	0.83[TSI][hapmap]
rs10082147	0.80[EUR][1000 genomes]
rs1028796	0.83[CHD][hapmap];0.97[GIH][hapmap];0.84[JPT][hapmap]
rs10864205	0.80[EUR][1000 genomes]
rs11120646	0.80[EUR][1000 genomes]
rs11120649	0.80[EUR][1000 genomes]
rs11120653	0.86[TSI][hapmap];0.84[YRI][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11120664	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11120666	0.81[ASW][hapmap];0.87[MKK][hapmap];0.83[TSI][hapmap];0.92[YRI][hapmap];0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11120686	0.83[CHD][hapmap];0.83[ASN][1000 genomes]
rs11579793	0.83[TSI][hapmap]
rs12029340	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12043203	0.80[EUR][1000 genomes]
rs12046040	0.81[EUR][1000 genomes]
rs12049039	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12049485	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12734222	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1538638	0.90[JPT][hapmap]
rs1547765	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1934429	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1934431	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1934432	0.82[EUR][1000 genomes]
rs1972368	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2027355	0.86[TSI][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2147912	0.81[CHD][hapmap];0.84[ASN][1000 genomes]
rs2364866	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28477637	0.81[EUR][1000 genomes]
rs4129019	0.83[CEU][hapmap]
rs4143467	0.97[AFR][1000 genomes]
rs4390149	0.83[TSI][hapmap]
rs4528089	0.80[EUR][1000 genomes]
rs4531267	0.89[CHB][hapmap];0.94[JPT][hapmap]
rs4607850	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6540912	0.83[TSI][hapmap]
rs6701765	0.85[MKK][hapmap]
rs7516792	0.80[EUR][1000 genomes]
rs7556611	0.81[TSI][hapmap];0.80[EUR][1000 genomes]
rs9887827	0.83[TSI][hapmap];0.80[EUR][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	nsv430324	chr1:215649163-216082605	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1006504	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv535288	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv949671	chr1:215942740-216120815	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv549192	chr1:215967857-216034753	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1012279	chr1:215982058-216035558	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv832548	chr1:215987089-216175724	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr1:216008400-216018000	Weak transcription	Osteobl	bone
2	chr1:216016600-216018000	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr1:216016600-216018600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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