Variant report

Variant	rs3851358
Chromosome Location	chr3:159137759-159137760
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs11706209	0.82[AMR][1000 genomes]
rs11707957	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11715734	1.00[CEU][hapmap]
rs1375403	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs1375404	0.87[EUR][1000 genomes]
rs1375405	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs1448998	1.00[CEU][hapmap];1.00[GIH][hapmap];0.93[TSI][hapmap]
rs1449012	0.96[CEU][hapmap]
rs1449024	1.00[CEU][hapmap]
rs1449027	0.81[CEU][hapmap]
rs1562671	1.00[CEU][hapmap]
rs1562672	0.92[CEU][hapmap];0.86[GIH][hapmap]
rs17795566	0.92[CEU][hapmap]
rs1975601	0.92[CEU][hapmap];0.86[GIH][hapmap]
rs2595232	0.81[CEU][hapmap]
rs2595236	0.81[CEU][hapmap]
rs2595243	0.92[CEU][hapmap];0.86[GIH][hapmap]
rs2595244	0.92[CEU][hapmap]
rs2595245	0.92[CEU][hapmap]
rs2595246	0.89[CEU][hapmap];0.83[GIH][hapmap]
rs2595247	0.92[CEU][hapmap]
rs2595248	0.89[CEU][hapmap];0.80[GIH][hapmap]
rs2621290	0.89[CEU][hapmap]
rs2621294	0.81[CEU][hapmap]
rs2621295	0.81[CEU][hapmap]
rs2621297	0.92[CEU][hapmap];0.83[GIH][hapmap]
rs2621299	0.92[CEU][hapmap]
rs2621300	0.92[CEU][hapmap]
rs2621310	0.92[CEU][hapmap];0.89[GIH][hapmap]
rs2621312	0.89[CEU][hapmap];0.86[GIH][hapmap]
rs2621313	0.92[CEU][hapmap]
rs2621314	0.92[CEU][hapmap];0.86[GIH][hapmap]
rs4680500	0.96[CEU][hapmap];1.00[GIH][hapmap];0.95[TSI][hapmap]
rs4680504	0.92[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.93[TSI][hapmap];0.82[YRI][hapmap]
rs4680505	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6441255	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs6782867	1.00[CEU][hapmap]
rs6790560	1.00[CEU][hapmap]
rs6807076	1.00[CEU][hapmap];1.00[GIH][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73166247	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs733904	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7428369	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7646959	1.00[CEU][hapmap];1.00[GIH][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7649056	1.00[CEU][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];0.98[TSI][hapmap]
rs9809743	0.81[YRI][hapmap]
rs9838071	0.81[YRI][hapmap]
rs9875283	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530059	chr3:158332590-159147549	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats 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	31 gene(s)	inside rSNPs	diseases
2	nsv470971	chr3:158590928-159158217	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv998949	chr3:158774806-159394550	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1004990	chr3:159090974-159174954	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	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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