Variant report

Variant	rs9350793
Chromosome Location	chr6:63921853-63921854
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10455121	0.90[ASN][1000 genomes]
rs10455353	0.95[CHB][hapmap];0.87[JPT][hapmap]
rs10755381	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs10755382	0.81[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10943590	0.94[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10943630	0.89[ASN][1000 genomes]
rs10943631	0.89[ASN][1000 genomes]
rs13198129	0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs13211975	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs13212822	0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs1504372	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs16893871	0.84[YRI][hapmap]
rs16893875	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1870488	0.83[YRI][hapmap]
rs2347253	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs2347255	0.92[ASN][1000 genomes]
rs3857526	0.85[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs4035415	0.88[ASN][1000 genomes]
rs4506024	0.87[ASN][1000 genomes]
rs4634433	0.84[YRI][hapmap]
rs61481123	0.93[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs6922948	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap]
rs6923494	0.87[ASN][1000 genomes]
rs6927705	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.92[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs6940141	0.90[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs7768652	0.80[YRI][hapmap]
rs9294135	0.90[ASN][1000 genomes]
rs9343837	0.94[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs9343839	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs9343842	0.90[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs9343866	0.88[ASN][1000 genomes]
rs9343888	0.81[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs9350790	0.89[YRI][hapmap]
rs9352711	0.89[ASN][1000 genomes]
rs9359356	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs9361456	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs9361463	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs9361500	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9361514	0.81[AFR][1000 genomes];0.88[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	nsv1019831	chr6:63279677-64230736	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1025099	chr6:63514227-64055649	Genic enhancers Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv538270	chr6:63682752-64147241	Flanking Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	esv2758058	chr6:63706622-63985889	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv2759434	chr6:63706622-63985889	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv830673	chr6:63833563-63939177	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv33308	chr6:63919357-63956379	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv970132	chr6:63920373-63922769	Inactive region	TF binding region CpG island	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
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