Variant report

Variant	rs2168103
Chromosome Location	chr6:81295573-81295574
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10447325	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10447326	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10806194	0.88[EUR][1000 genomes]
rs10943720	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10943724	0.93[ASN][1000 genomes]
rs10943725	0.92[ASN][1000 genomes]
rs10943726	0.91[ASN][1000 genomes]
rs12195284	0.87[EUR][1000 genomes]
rs12195347	0.88[EUR][1000 genomes]
rs1454446	0.93[ASN][1000 genomes]
rs1454465	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs1454466	0.85[EUR][1000 genomes]
rs2247639	0.88[EUR][1000 genomes]
rs2322842	0.87[EUR][1000 genomes]
rs2322843	0.87[EUR][1000 genomes]
rs2603458	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2653484	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28360539	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28789711	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2917600	0.88[EUR][1000 genomes]
rs4315973	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4394171	0.87[EUR][1000 genomes]
rs4410688	0.87[EUR][1000 genomes]
rs4527663	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs471335	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs480295	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs541037	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs541841	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs546848	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs549621	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62406533	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs667882	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs683706	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6915595	0.93[ASN][1000 genomes]
rs6933382	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6936716	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs722715	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9449074	0.88[EUR][1000 genomes]
rs953498	0.87[EUR][1000 genomes]
rs953499	0.87[EUR][1000 genomes]
rs953500	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531333	chr6:81042427-81836484	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1019670	chr6:81086504-81569984	ZNF genes & repeats Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv915714	chr6:81134888-81366749	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv886312	chr6:81166178-81309481	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv998220	chr6:81258085-81298829	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv522523	chr6:81262988-81298688	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv2757182	chr6:81265495-81304211	Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	esv2759448	chr6:81265495-81304211	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv518724	chr6:81284507-81298688	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	nsv1020533	chr6:81288890-81406533	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv538340	chr6:81288890-81406533	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv508417	chr6:81290516-81330590	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:81294800-81317000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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