Variant report

Variant	rs4765767
Chromosome Location	chr12:4199676-4199677
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10848976	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10848978	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10848979	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10848983	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10848984	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11062989	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11062992	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11062999	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11063000	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11063003	0.81[AMR][1000 genomes]
rs11063004	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11063007	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11063008	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11063009	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12228949	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12229320	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12230013	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12231207	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12579541	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12579556	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12579813	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2072497	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2110592	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2160160	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2160161	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2358594	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2358836	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2358837	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2540139	0.98[EUR][1000 genomes]
rs3889565	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4765762	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4765769	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4766207	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4766208	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4766209	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4766211	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs58334161	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs59759498	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs60789908	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6489518	0.85[EUR][1000 genomes]
rs7136346	0.85[EUR][1000 genomes]
rs741243	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs759306	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7969060	0.84[AMR][1000 genomes]
rs7975418	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9634153	0.90[AMR][1000 genomes];0.85[EUR][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	nsv530520	chr12:3726841-4601757	Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:4189800-4201000	Weak transcription	Pancreas	Pancrea
2	chr12:4193000-4201200	Weak transcription	Lung	lung
3	chr12:4194800-4200000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:4196800-4201200	Enhancers	Fetal Stomach	stomach
5	chr12:4198000-4200000	Weak transcription	Placenta	Placenta
6	chr12:4198200-4200600	Enhancers	Fetal Heart	heart
7	chr12:4198600-4200200	Weak transcription	Adipose Nuclei	Adipose
8	chr12:4199000-4200400	Weak transcription	Fetal Muscle Trunk	muscle
9	chr12:4199200-4200200	Weak transcription	Fetal Muscle Leg	muscle
10	chr12:4199200-4200400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr12:4199200-4200600	Weak transcription	Fetal Lung	lung

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