Variant report

Variant	rs796644
Chromosome Location	chr2:125049683-125049684
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10496635	0.81[JPT][hapmap]
rs11123030	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs1170578	0.94[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs1170605	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs1170606	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs1170610	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs1170615	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs1170616	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs1170617	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs1170622	0.84[CHB][hapmap];0.81[JPT][hapmap]
rs1170623	0.84[CHB][hapmap]
rs1170624	0.85[CHB][hapmap];0.81[JPT][hapmap]
rs1170625	0.85[CHB][hapmap];0.82[JPT][hapmap]
rs1170627	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs1170628	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs1170631	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs1186066	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs1186396	0.80[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs2163249	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs2565770	0.89[YRI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2699362	0.90[ASN][1000 genomes]
rs2699363	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6541945	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs707498	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7560777	0.81[CHB][hapmap];0.87[JPT][hapmap]
rs779976	0.80[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs779977	0.80[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs779985	0.80[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap]
rs779994	0.85[CHB][hapmap];0.82[JPT][hapmap]
rs779995	0.80[CEU][hapmap];0.85[CHB][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes]
rs779996	0.81[EUR][1000 genomes]
rs779997	0.81[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs780020	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs780023	0.94[CHB][hapmap];0.85[JPT][hapmap];0.98[ASN][1000 genomes]
rs780024	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs780025	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs780026	0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs780027	0.89[ASN][1000 genomes]
rs780028	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs780029	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs780030	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs780031	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs780032	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs780033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs780034	1.00[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs780035	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs780042	0.81[EUR][1000 genomes]
rs780044	0.81[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs780050	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs780051	0.85[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs780052	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs796643	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs810513	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs811901	0.81[EUR][1000 genomes]
rs891410	0.85[CHB][hapmap];0.82[JPT][hapmap]
rs9308649	0.94[YRI][hapmap];0.80[AFR][1000 genomes]
rs9646914	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874989	chr2:124892592-125176030	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv874990	chr2:125038678-125099924	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No data

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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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