Variant report

Variant	rs73293935
Chromosome Location	chr14:70951533-70951534
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs12232170	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12436902	0.91[EUR][1000 genomes]
rs12586325	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12586328	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17107997	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17108176	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1953798	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1953802	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1959483	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1959484	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1959486	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2095807	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2293877	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2332389	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34512695	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4902827	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56778245	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56824265	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57146008	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61671382	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7143655	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7145265	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7152771	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7154884	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7159432	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73293909	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8014338	0.89[EUR][1000 genomes]
rs8015163	0.91[EUR][1000 genomes]
rs8017584	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8021308	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[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	nsv565042	chr14:70951234-71011734	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70910600-70955600	Weak transcription	Left Ventricle	heart
2	chr14:70948000-70955000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr14:70949000-70956000	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr14:70949200-70956400	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr14:70949400-70956200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr14:70951200-70956200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr14:70951400-70955000	Weak transcription	Aorta	Aorta
8	chr14:70951400-70957600	Weak transcription	Skeletal Muscle Female	skeletal muscle

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