Variant report

Variant	rs1335919
Chromosome Location	chr1:221018385-221018386
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10495152	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10863567	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10863568	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11118609	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11118611	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11118615	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11118616	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11118619	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12057411	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12073837	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12089958	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12117818	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12123589	0.91[AFR][1000 genomes]
rs12129004	0.88[CEU][hapmap];0.80[EUR][1000 genomes]
rs12139139	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12145674	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1494368	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1494371	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1494372	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17008806	0.95[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs17596850	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17650107	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2242358	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs2279638	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2378425	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2642421	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs35730037	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4143773	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61830270	0.84[ASN][1000 genomes]
rs61830289	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6541161	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6668666	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6673877	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6693017	0.89[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs7530074	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7530176	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7530493	0.93[ASN][1000 genomes]
rs7544735	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7553447	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs881995	0.95[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs903319	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs984676	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221015600-221018400	Enhancers	Fetal Heart	heart
2	chr1:221017800-221018400	Enhancers	Right Atrium	heart
3	chr1:221018000-221018400	Enhancers	Right Ventricle	heart

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