Variant report

Variant	rs4449324
Chromosome Location	chr3:68231687-68231688
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1007583	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13068860	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs1388492	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1388493	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1491736	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1866290	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2396322	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2396323	0.81[CEU][hapmap]
rs4241393	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs4276186	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4446218	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4447769	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4459906	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4478080	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4855495	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4855497	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6794104	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs6806747	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7628811	0.81[CEU][hapmap]
rs7635281	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7650009	0.94[CHB][hapmap];0.94[JPT][hapmap]
rs9814953	0.92[CHB][hapmap];0.85[JPT][hapmap]
rs9818217	1.00[CEU][hapmap]
rs9843449	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

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	nsv1002010	chr3:67785913-68312064	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1009871	chr3:67862617-68312064	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv536583	chr3:67862617-68312064	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	esv2752014	chr3:68091879-68416989	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv1007450	chr3:68094416-68346546	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv876925	chr3:68180422-68288626	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv876926	chr3:68204939-68282529	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	TF binding region 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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