Variant report

Variant	rs67545147
Chromosome Location	chr8:113691417-113691418
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1019603	0.85[EUR][1000 genomes]
rs10505190	0.85[EUR][1000 genomes]
rs10505191	0.85[EUR][1000 genomes]
rs10505192	0.85[EUR][1000 genomes]
rs10505193	0.85[EUR][1000 genomes]
rs10955633	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12114545	0.82[EUR][1000 genomes]
rs12114638	0.82[EUR][1000 genomes]
rs12677918	0.85[EUR][1000 genomes]
rs12679365	0.85[EUR][1000 genomes]
rs12682342	0.82[EUR][1000 genomes]
rs1549351	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1549352	0.84[EUR][1000 genomes]
rs1549353	0.84[EUR][1000 genomes]
rs16884004	0.85[EUR][1000 genomes]
rs16884034	0.85[EUR][1000 genomes]
rs16884039	0.84[EUR][1000 genomes]
rs16884044	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16884046	0.83[EUR][1000 genomes]
rs1863088	0.84[EUR][1000 genomes]
rs1991134	0.84[EUR][1000 genomes]
rs1991135	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2052635	0.84[EUR][1000 genomes]
rs2194597	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4582593	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4876291	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4876292	0.85[EUR][1000 genomes]
rs4876293	0.85[EUR][1000 genomes]
rs4876483	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4876484	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4876492	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56859083	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61498012	0.84[EUR][1000 genomes]
rs6469435	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6469436	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs66817037	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67112531	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs67594301	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs67838088	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs68078492	0.84[EUR][1000 genomes]
rs6993756	0.82[EUR][1000 genomes]
rs7002262	0.85[EUR][1000 genomes]
rs7820108	0.85[EUR][1000 genomes]
rs7820337	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7826958	0.85[EUR][1000 genomes]
rs7837037	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7845849	0.81[EUR][1000 genomes]
rs9649935	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9650049	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9918857	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533857	chr8:112819659-113801258	Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1022457	chr8:113071774-113811177	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	esv2753595	chr8:113283214-114190390	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv831427	chr8:113494319-113699264	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
5	nsv534270	chr8:113585830-113979075	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	3 gene(s)	inside rSNPs	diseases
6	nsv891324	chr8:113647451-113732965	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:113687000-113699200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:113691400-113692200	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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