Variant report

Variant	rs9376698
Chromosome Location	chr6:142940262-142940263
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10484589	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11968407	1.00[EUR][1000 genomes]
rs12663303	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17071903	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17071909	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1876842	0.86[ASN][1000 genomes]
rs1876844	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2136517	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2136518	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2136519	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2175164	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55671842	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55702719	0.83[EUR][1000 genomes]
rs55747254	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55749277	1.00[EUR][1000 genomes]
rs55767236	0.83[EUR][1000 genomes]
rs55787572	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55889677	0.89[EUR][1000 genomes]
rs56017506	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56019737	1.00[EUR][1000 genomes]
rs56043044	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56049518	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56055844	1.00[EUR][1000 genomes]
rs56082312	1.00[EUR][1000 genomes]
rs56135811	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56196468	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56216981	0.89[EUR][1000 genomes]
rs56228013	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56267414	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56358606	1.00[EUR][1000 genomes]
rs56363136	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6914176	0.84[ASN][1000 genomes]
rs6924746	0.85[CHB][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs6929406	0.86[ASN][1000 genomes]
rs6936988	0.84[ASN][1000 genomes]
rs72982458	0.89[EUR][1000 genomes]
rs72982478	0.83[EUR][1000 genomes]
rs72984344	0.83[EUR][1000 genomes]
rs72984346	0.83[EUR][1000 genomes]
rs72984357	0.83[EUR][1000 genomes]
rs72994122	0.89[EUR][1000 genomes]
rs72994141	0.89[EUR][1000 genomes]
rs72996359	1.00[EUR][1000 genomes]
rs72996364	1.00[EUR][1000 genomes]
rs72996365	0.90[EUR][1000 genomes]
rs72998326	1.00[EUR][1000 genomes]
rs72998327	1.00[EUR][1000 genomes]
rs72998328	1.00[EUR][1000 genomes]
rs72998329	1.00[EUR][1000 genomes]
rs72998335	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998337	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998353	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998356	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998364	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998367	1.00[EUR][1000 genomes]
rs72998369	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998371	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998375	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998382	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998384	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998386	1.00[EUR][1000 genomes]
rs72998388	0.94[EUR][1000 genomes]
rs72998391	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998393	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998399	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998400	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72998402	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7749392	0.84[ASN][1000 genomes]
rs7753433	0.85[CHB][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs7757435	0.84[ASN][1000 genomes]
rs7759477	1.00[EUR][1000 genomes]
rs7760316	0.84[ASN][1000 genomes]
rs7772506	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7772807	0.84[ASN][1000 genomes]
rs9373356	0.89[ASN][1000 genomes]
rs9376700	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9376702	0.84[ASN][1000 genomes]
rs9376703	0.84[ASN][1000 genomes]
rs9386004	0.89[ASN][1000 genomes]
rs9386005	0.85[CHB][hapmap];0.89[ASN][1000 genomes]
rs9403402	0.85[CHB][hapmap];0.85[JPT][hapmap];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1023426	chr6:142813845-142940262	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830827	chr6:142840734-143015005	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142933600-142944000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:142938800-142945800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:142939200-142943800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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