Variant report

Variant	rs10929472
Chromosome Location	chr2:7374639-7374640
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10929471	0.91[ASN][1000 genomes]
rs10929473	0.89[ASN][1000 genomes]
rs10929474	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11682417	0.90[ASN][1000 genomes]
rs11687207	0.85[ASN][1000 genomes]
rs12612059	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12619070	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12999068	0.80[ASN][1000 genomes]
rs13013964	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1404845	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1464880	0.80[ASN][1000 genomes]
rs1473655	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1525490	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1525492	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs16866007	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs16866008	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs16866010	0.84[ASN][1000 genomes]
rs1880605	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1917678	0.80[ASN][1000 genomes]
rs34325684	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4233854	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4265983	0.85[ASN][1000 genomes]
rs4668531	0.90[ASN][1000 genomes]
rs4669153	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4669156	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4669158	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4669164	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4669169	0.93[ASN][1000 genomes]
rs55869666	0.86[ASN][1000 genomes]
rs7559257	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs872442	0.85[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	nsv915888	chr2:7197783-7461967	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1000136	chr2:7337270-7379211	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	nsv833337	chr2:7337273-7521146	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:7372000-7388400	Weak transcription	Pancreas	Pancrea

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