Variant report

Variant	rs1754271
Chromosome Location	chr10:25692874-25692875
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 112 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:109)

rs_ID	r²[population]
rs10508694	0.82[ASN][1000 genomes]
rs10764543	0.82[ASN][1000 genomes]
rs10828791	0.82[ASN][1000 genomes]
rs10828792	0.82[ASN][1000 genomes]
rs10828793	0.82[ASN][1000 genomes]
rs11014527	0.82[ASN][1000 genomes]
rs11014528	0.81[ASN][1000 genomes]
rs11014529	0.82[ASN][1000 genomes]
rs11014530	0.82[ASN][1000 genomes]
rs1122775	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1122776	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11818261	0.82[ASN][1000 genomes]
rs12240665	0.82[ASN][1000 genomes]
rs12249852	0.82[ASN][1000 genomes]
rs12251868	0.82[ASN][1000 genomes]
rs12251917	0.82[ASN][1000 genomes]
rs12254479	0.82[ASN][1000 genomes]
rs12256778	0.82[ASN][1000 genomes]
rs12256851	0.82[ASN][1000 genomes]
rs12258359	0.82[ASN][1000 genomes]
rs12258665	0.82[ASN][1000 genomes]
rs12258671	0.82[ASN][1000 genomes]
rs12259043	0.82[ASN][1000 genomes]
rs12259696	0.82[ASN][1000 genomes]
rs12358447	0.82[ASN][1000 genomes]
rs12764320	0.82[ASN][1000 genomes]
rs12766749	0.82[ASN][1000 genomes]
rs1329264	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1329265	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1341963	1.00[ASN][1000 genomes]
rs1341964	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1341966	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1576317	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1576318	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1576320	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1576321	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1590836	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1591249	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1591250	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1612200	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1626372	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1628986	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1630323	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1632593	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1754253	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1754254	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1754255	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1754256	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1754257	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1754258	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1754260	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1754264	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1754265	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1754268	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1754269	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1760716	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1760726	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1760727	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1760728	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1760729	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1760730	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1760733	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1760734	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1760735	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1760755	0.83[ASN][1000 genomes]
rs1760758	0.88[ASN][1000 genomes]
rs1760759	0.88[ASN][1000 genomes]
rs1760762	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1760763	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1760764	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1760765	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1773607	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1773608	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1773609	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1773612	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1773614	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1773616	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1773618	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1773622	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1773623	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1773648	0.83[ASN][1000 genomes]
rs1773649	0.84[ASN][1000 genomes]
rs1773650	0.84[ASN][1000 genomes]
rs1773651	0.83[ASN][1000 genomes]
rs1773689	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1773690	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2262989	0.83[ASN][1000 genomes]
rs2807245	0.84[ASN][1000 genomes]
rs35663899	0.82[ASN][1000 genomes]
rs35973294	0.82[ASN][1000 genomes]
rs4351726	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs476972	0.83[ASN][1000 genomes]
rs489052	0.84[ASN][1000 genomes]
rs489186	0.84[ASN][1000 genomes]
rs495338	0.84[ASN][1000 genomes]
rs495456	0.84[ASN][1000 genomes]
rs516071	0.84[ASN][1000 genomes]
rs518751	0.80[ASN][1000 genomes]
rs541206	0.84[ASN][1000 genomes]
rs573812	0.84[ASN][1000 genomes]
rs7090972	0.82[ASN][1000 genomes]
rs7091686	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7094439	0.82[ASN][1000 genomes]
rs824590	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs824592	0.88[ASN][1000 genomes]
rs824593	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs824597	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824598	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs824599	0.82[AFR][1000 genomes];1.00[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	esv2761583	chr10:25525657-25722444	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv550226	chr10:25653017-25693426	ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25687200-25697800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr10:25692800-25693400	Enhancers	Pancreatic Islets	Pancreatic Islet

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