Variant report

Variant	rs1151776
Chromosome Location	chr1:62201203-62201204
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs11207807	0.88[EUR][1000 genomes]
rs11207808	0.92[EUR][1000 genomes]
rs1151756	0.92[EUR][1000 genomes]
rs1151757	0.92[EUR][1000 genomes]
rs1151759	0.92[EUR][1000 genomes]
rs1151762	0.91[EUR][1000 genomes]
rs1151770	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1151771	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1151773	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1151775	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12117475	0.88[EUR][1000 genomes]
rs12124430	0.88[EUR][1000 genomes]
rs12130241	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12130439	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12134102	0.88[EUR][1000 genomes]
rs12134205	0.88[EUR][1000 genomes]
rs12134428	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12137410	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12141280	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12141298	0.88[EUR][1000 genomes]
rs12144284	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1286624	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1286625	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1286626	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1286628	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1286629	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1286630	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1286634	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1611797	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1620169	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1692131	0.88[EUR][1000 genomes]
rs17378384	0.88[EUR][1000 genomes]
rs1779267	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2051135	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2051136	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2799626	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4443919	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6666057	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6691402	0.91[EUR][1000 genomes]
rs6697770	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72672375	0.80[EUR][1000 genomes]
rs72672390	0.88[EUR][1000 genomes]
rs72674608	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7536565	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7538825	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7539026	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7550631	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1000294	chr1:61746280-62350718	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62191400-62207400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:62201200-62202200	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr1:62201200-62202200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr1:62201200-62203000	Enhancers	Primary T helper cells fromperipheralblood	blood

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