Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1323428	0.80[ASN][1000 genomes]
rs1337677	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1337683	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1337710	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1415646	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1415651	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1832334	0.85[EUR][1000 genomes]
rs2065964	0.82[EUR][1000 genomes]
rs2152866	0.86[ASN][1000 genomes]
rs2210991	0.91[ASN][1000 genomes]
rs2210993	0.85[ASN][1000 genomes]
rs2485524	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2485526	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2485529	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2485530	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2485532	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2485535	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2506351	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2506358	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2506360	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2506361	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2506363	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4742822	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7390803	0.82[EUR][1000 genomes]
rs7849059	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs945870	0.86[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	nsv1046975	chr9:104167583-104659873	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv949579	chr9:104229820-104512923	Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv831672	chr9:104300755-104480849	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv1046590	chr9:104450624-104848588	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104478200-104480800	Enhancers	Fetal Lung	lung
2	chr9:104479000-104482400	Enhancers	Fetal Muscle Leg	muscle
3	chr9:104479200-104480200	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr9:104479200-104480400	Weak transcription	Fetal Kidney	kidney
5	chr9:104479600-104480000	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr9:104479800-104481200	Enhancers	Pancreatic Islets	Pancreatic Islet

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