Variant report

Variant	rs7739226
Chromosome Location	chr6:75370913-75370914
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs12527794	0.84[ASN][1000 genomes]
rs12528062	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12529893	0.84[ASN][1000 genomes]
rs1537950	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2065884	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2095613	0.95[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs2152712	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2152713	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2243712	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2252269	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2252270	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2252276	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2485067	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2485076	0.85[AFR][1000 genomes]
rs2485077	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2485078	0.86[AFR][1000 genomes]
rs2485080	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2485081	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2485082	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2485083	0.83[AFR][1000 genomes]
rs2485084	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2485085	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2485086	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2485087	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2485088	0.86[AFR][1000 genomes]
rs2485089	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2485091	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2485092	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2485093	0.93[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2485094	0.85[ASN][1000 genomes]
rs2485096	0.95[AFR][1000 genomes];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2502468	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2502470	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2502473	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2502474	0.93[AFR][1000 genomes];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2502475	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2502477	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2502478	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2502481	0.82[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs2502482	0.89[AFR][1000 genomes]
rs2502484	0.89[AFR][1000 genomes]
rs2502485	0.86[AFR][1000 genomes]
rs2502486	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2502487	0.86[AFR][1000 genomes]
rs2502488	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2502489	0.92[ASN][1000 genomes]
rs2502490	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2502491	0.86[AFR][1000 genomes]
rs2502492	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2502493	0.85[AFR][1000 genomes]
rs2502494	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2502503	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2502505	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2502533	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2502537	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9343210	0.84[ASN][1000 genomes]
rs9360837	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520746	chr6:75211546-75691814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv917283	chr6:75234428-75641440	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv830694	chr6:75245483-75446282	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1027029	chr6:75364848-75417967	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1015675	chr6:75365189-75422887	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	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	chr6:75368000-75371000	Weak transcription	NHDF-Ad	bronchial

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