Variant report

Variant	rs13280010
Chromosome Location	chr8:35263739-35263740
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 117 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs10086433	0.97[ASN][1000 genomes]
rs10091291	0.93[ASN][1000 genomes]
rs10097983	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10101937	0.93[ASN][1000 genomes]
rs10104660	0.95[ASN][1000 genomes]
rs10108964	0.97[ASN][1000 genomes]
rs10110454	0.96[ASN][1000 genomes]
rs10113220	0.97[ASN][1000 genomes]
rs10503979	1.00[ASN][1000 genomes]
rs10954985	0.97[ASN][1000 genomes]
rs10954986	0.97[ASN][1000 genomes]
rs10954987	1.00[ASN][1000 genomes]
rs1112204	0.83[ASN][1000 genomes]
rs11984839	0.95[ASN][1000 genomes]
rs11991431	0.92[ASN][1000 genomes]
rs11991965	0.97[ASN][1000 genomes]
rs11992772	0.97[ASN][1000 genomes]
rs11993717	0.83[ASN][1000 genomes]
rs11996793	0.96[ASN][1000 genomes]
rs11997743	1.00[ASN][1000 genomes]
rs12056409	0.97[ASN][1000 genomes]
rs12541372	0.97[ASN][1000 genomes]
rs12542495	0.97[ASN][1000 genomes]
rs12542606	0.80[ASN][1000 genomes]
rs12545700	0.83[ASN][1000 genomes]
rs12550658	0.97[ASN][1000 genomes]
rs12680114	0.97[ASN][1000 genomes]
rs13250741	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13266519	1.00[ASN][1000 genomes]
rs13282296	0.89[ASN][1000 genomes]
rs13282746	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1358563	0.97[ASN][1000 genomes]
rs1358564	0.97[ASN][1000 genomes]
rs1406376	0.97[ASN][1000 genomes]
rs1528704	0.99[ASN][1000 genomes]
rs1528705	0.99[ASN][1000 genomes]
rs1528708	0.97[ASN][1000 genomes]
rs1528709	0.98[ASN][1000 genomes]
rs1528710	1.00[ASN][1000 genomes]
rs1528716	0.96[ASN][1000 genomes]
rs1528717	0.97[ASN][1000 genomes]
rs1528718	0.97[ASN][1000 genomes]
rs1528719	0.97[ASN][1000 genomes]
rs1534584	1.00[ASN][1000 genomes]
rs1534587	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1554864	0.97[ASN][1000 genomes]
rs1590092	0.91[ASN][1000 genomes]
rs1590093	0.93[ASN][1000 genomes]
rs1609345	1.00[ASN][1000 genomes]
rs16883904	1.00[ASN][1000 genomes]
rs1919336	0.97[ASN][1000 genomes]
rs1919337	0.97[ASN][1000 genomes]
rs1919346	0.97[ASN][1000 genomes]
rs1919349	0.97[ASN][1000 genomes]
rs1919355	0.97[ASN][1000 genomes]
rs1950042	0.84[ASN][1000 genomes]
rs1980396	1.00[ASN][1000 genomes]
rs2204719	0.97[ASN][1000 genomes]
rs2405735	0.97[ASN][1000 genomes]
rs28388271	0.97[ASN][1000 genomes]
rs28395502	0.97[ASN][1000 genomes]
rs28412900	0.97[ASN][1000 genomes]
rs2950892	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2950893	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2950895	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2950897	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2950898	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2950901	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2950909	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2950924	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2980378	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2980391	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2980403	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2980406	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2980408	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3108619	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35169691	0.98[ASN][1000 genomes]
rs35365523	0.97[ASN][1000 genomes]
rs35985268	0.93[ASN][1000 genomes]
rs3744	0.83[ASN][1000 genomes]
rs4255132	0.83[ASN][1000 genomes]
rs4360290	0.97[ASN][1000 genomes]
rs4452796	1.00[ASN][1000 genomes]
rs4492371	0.94[ASN][1000 genomes]
rs4540403	0.93[ASN][1000 genomes]
rs4739302	0.97[ASN][1000 genomes]
rs4739304	0.97[ASN][1000 genomes]
rs4739399	0.84[ASN][1000 genomes]
rs4739400	0.89[ASN][1000 genomes]
rs4739402	0.97[ASN][1000 genomes]
rs4739408	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs5000056	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58886150	0.99[ASN][1000 genomes]
rs6468316	0.92[ASN][1000 genomes]
rs6468317	1.00[ASN][1000 genomes]
rs6991984	0.94[ASN][1000 genomes]
rs6992809	0.97[ASN][1000 genomes]
rs6997453	0.97[ASN][1000 genomes]
rs7006157	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7013157	1.00[ASN][1000 genomes]
rs7815710	0.81[ASN][1000 genomes]
rs7817194	0.97[ASN][1000 genomes]
rs7819547	0.96[ASN][1000 genomes]
rs7824855	0.95[ASN][1000 genomes]
rs7827072	0.97[ASN][1000 genomes]
rs7827646	1.00[ASN][1000 genomes]
rs7829022	0.98[ASN][1000 genomes]
rs7829585	1.00[ASN][1000 genomes]
rs7839131	1.00[ASN][1000 genomes]
rs871994	0.97[ASN][1000 genomes]
rs9297236	0.93[ASN][1000 genomes]
rs9297237	0.97[ASN][1000 genomes]
rs951515	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017085	chr8:34742896-35594241	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv539546	chr8:34742896-35594241	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv520421	chr8:35155517-35479468	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv890717	chr8:35184361-35315188	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs13280010	ASH2L	cis	parietal	SCAN
rs13280010	LETM2	cis	cerebellum	SCAN
rs13280010	UNC5D	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:35254000-35269000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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