Variant report

Variant	rs55895997
Chromosome Location	chr3:146463291-146463292
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1003263	0.89[ASN][1000 genomes]
rs1003264	0.89[ASN][1000 genomes]
rs1019897	0.85[ASN][1000 genomes]
rs10935642	0.89[ASN][1000 genomes]
rs11705960	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12497166	0.96[ASN][1000 genomes]
rs1397886	0.82[ASN][1000 genomes]
rs1549838	0.85[ASN][1000 genomes]
rs1606177	0.96[ASN][1000 genomes]
rs1606178	0.96[ASN][1000 genomes]
rs17371141	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17701818	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1991715	0.80[ASN][1000 genomes]
rs2174783	0.84[ASN][1000 genomes]
rs28493260	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28624889	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28885973	0.96[ASN][1000 genomes]
rs3843364	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4681336	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56887948	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58890956	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62272988	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6440455	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6440458	0.87[ASN][1000 genomes]
rs6440459	0.85[ASN][1000 genomes]
rs6440460	0.85[ASN][1000 genomes]
rs6762735	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6808136	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7619766	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7638634	0.87[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs9289731	0.87[AFR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9289732	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs961897	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs981484	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9828677	0.84[ASN][1000 genomes]
rs9831862	0.85[ASN][1000 genomes]
rs9834967	0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs9835606	0.85[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs9840734	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9841610	0.85[ASN][1000 genomes]
rs9841625	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9841883	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9842074	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9845940	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9856265	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9857850	0.86[ASN][1000 genomes]
rs9861781	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9861946	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv516386	chr3:146366513-146758405	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv591961	chr3:146394094-146725217	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1007875	chr3:146401461-146776618	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv877624	chr3:146414837-146536741	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv998040	chr3:146416916-146729962	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv536760	chr3:146416916-146729962	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv1001931	chr3:146419061-146745361	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv877625	chr3:146461435-146521978	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146462400-146463400	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr3:146462400-146463400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr3:146462600-146464000	Weak transcription	Dnd41	blood
4	chr3:146462600-146464000	Weak transcription	HMEC	breast

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