Variant report

Variant	rs61885269
Chromosome Location	chr11:25931932-25931933
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1025837	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1025839	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10400312	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10400315	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11029003	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11602363	0.81[ASN][1000 genomes]
rs12417352	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12417638	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12417956	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12418056	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12418534	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12418764	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1348166	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1441494	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1441510	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs167877	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16914877	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs179189	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1837782	0.90[ASN][1000 genomes]
rs184494	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1971144	0.87[ASN][1000 genomes]
rs2249568	0.80[ASN][1000 genomes]
rs2249717	0.81[ASN][1000 genomes]
rs228189	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2349603	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs328464	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs328467	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs328468	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs328469	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs328484	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs328487	0.81[ASN][1000 genomes]
rs328488	0.81[ASN][1000 genomes]
rs4291637	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61885271	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61885276	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61885280	0.81[ASN][1000 genomes]
rs61888163	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7101988	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7104555	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7125344	0.92[ASN][1000 genomes]
rs7935268	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7947256	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs894174	0.80[ASN][1000 genomes]
rs971386	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760599	chr11:25186984-26159450	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1046507	chr11:25469712-26111707	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv832091	chr11:25823826-26009887	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv469948	chr11:25859783-26026233	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1041778	chr11:25898574-26098141	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv897140	chr11:25905509-25991194	Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv467775	chr11:25916225-25957544	Enhancers Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv553896	chr11:25916225-25957544	Enhancers Weak transcription Active TSS	TF binding 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	chr11:25930200-25932000	Enhancers	Fetal Lung	lung
2	chr11:25931800-25932200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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